Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US6465463 | AZURITY | Methods of treating and preventing congestive heart failure with hydralazine compounds and isosorbide dinitrate or isosorbide mononitrate |
Sep, 2020
(3 years ago) | |
US6784177 | AZURITY | Methods using hydralazine compounds and isosorbide dinitrate or isosorbide mononitrate |
Sep, 2020
(3 years ago) |
Drugs and Companies using HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE ingredient
Market Authorisation Date: 23 June, 2005
Treatment: Method of treatment of heart failure
Dosage: TABLET;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance. | ||||
US5583141 | AZURITY | Heterocyclic compounds and their use as angiotensin antagonists |
Dec, 2013
(10 years ago) | |
US7157584 | AZURITY | Benzimidazole derivative and use thereof |
May, 2025
(1 year, 1 month from now) | |
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US5958961 | AZURITY | Pharmaceutical composition for angiotensin II-mediated diseases |
Jun, 2014
(9 years ago) | |
US7572920 | AZURITY | Benzimidazole derivative and use as a II receptor antagonist |
Jan, 2025
(8 months from now) | |
US9066936 | AZURITY | Solid pharmaceutical composition comprising a benzimidazole-7-carboxylate derivative and a pH control agent |
Mar, 2028
(3 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
New Chemical Entity Exclusivity(NCE) | Feb 25, 2016 |
Drugs and Companies using AZILSARTAN KAMEDOXOMIL ingredient
NCE-1 date: 25 February, 2015
Market Authorisation Date: 25 February, 2011
Treatment: Treatment of hypertension
Dosage: TABLET;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance. | ||||
US5583141 | AZURITY | Heterocyclic compounds and their use as angiotensin antagonists |
Dec, 2013
(10 years ago) | |
US7157584 | AZURITY | Benzimidazole derivative and use thereof |
May, 2025
(1 year, 1 month from now) | |
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US7572920 | AZURITY | Benzimidazole derivative and use as a II receptor antagonist |
Jan, 2025
(8 months from now) | |
US9066936 | AZURITY | Solid pharmaceutical composition comprising a benzimidazole-7-carboxylate derivative and a pH control agent |
Mar, 2028
(3 years from now) | |
US9169238 | AZURITY | Solid pharmaceutical composition |
Feb, 2030
(5 years from now) | |
US9387249 | AZURITY | Methods of treating hypertension with at least one angiotensin II receptor blocker and chlorthalidone |
Jul, 2031
(7 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
New Combination(NC) | Dec 20, 2014 |
New Chemical Entity Exclusivity(NCE) | Feb 25, 2016 |
Drugs and Companies using AZILSARTAN KAMEDOXOMIL; CHLORTHALIDONE ingredient
NCE-1 date: 25 February, 2015
Market Authorisation Date: 20 December, 2011
Treatment: Treatment of hypertension
Dosage: TABLET;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10772868 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US9808442 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US10154987 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US9669008 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US11040023 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US10786482 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US11141405 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US11173141 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) | |
US10039745 | AZURITY | Enalapril formulations |
Mar, 2036
(11 years from now) |
Drugs and Companies using ENALAPRIL MALEATE ingredient
Market Authorisation Date: 20 September, 2016
Treatment: Treatment of hypertension; Treatment of heart failure
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11633374 | AZURITY | Compositions and methods for treating epilepsy, seizures and other conditions |
Aug, 2040
(16 years from now) | |
US11433046 | AZURITY | Compositions and methods for treating epilepsy, seizures and other conditions |
Aug, 2040
(16 years from now) | |
US11826343 | AZURITY | Compositions and methods for treating epilepsy, seizures and other conditions |
Aug, 2040
(16 years from now) |
Drugs and Companies using TOPIRAMATE ingredient
Market Authorisation Date: 05 November, 2021
Treatment: Indicated for the preventive treatment of migraine in patients 12 years and older
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10130580 | AZURITY | Taste-masked pharmaceutical compositions |
Apr, 2024
(6 hours ago) | |
US11160772 | AZURITY | Oral amphetamine composition |
Mar, 2037
(12 years from now) | |
US10441554 | AZURITY | Oral amphetamine composition |
Mar, 2037
(12 years from now) |
Drugs and Companies using AMPHETAMINE SULFATE ingredient
Market Authorisation Date: 16 April, 2021
Treatment: NA
Dosage: TABLET, ORALLY DISINTEGRATING;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10959948 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US10493028 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US11638692 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US10959947 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US10959949 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US10959946 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) | |
US10688046 | AZURITY | Composition and method for vancomycin oral liquid |
Mar, 2035
(10 years from now) |
Drugs and Companies using VANCOMYCIN HYDROCHLORIDE ingredient
Market Authorisation Date: 26 January, 2018
Treatment: Treatment of c. difficile-associated diarrhea
Dosage: FOR SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11446246 | AZURITY | Suspensions and diluents for metronidazole and baclofen |
Sep, 2037
(13 years from now) | |
US11324696 | AZURITY | Suspensions and diluents for metronidazole and baclofen |
Sep, 2037
(13 years from now) |
Drugs and Companies using BACLOFEN ingredient
Market Authorisation Date: 04 February, 2022
Treatment: Indicated for the treatment of spasticity resulting from multiple sclerosis
Dosage: SUSPENSION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents protects the active chemical substance. Only drug patent owner can launch products that use this active substance. | ||||
US8048917 | AZURITY | Prodrugs of GABA analogs, compositions and uses thereof |
Nov, 2022
(1 year, 5 months ago) | |
US6818787 | AZURITY | Prodrugs of GABA analogs, compositions and uses thereof |
Apr, 2025
(11 months from now) | |
US8026279 | AZURITY | Crystalline form of γ-aminobutyric acid analog |
Nov, 2026
(2 years from now) | |
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US8686034 | AZURITY | Crystalline form of γ-aminobutyric acid analog |
Jan, 2025
(9 months from now) | |
US8114909 | AZURITY | Treating or preventing restless legs syndrome using prodrugs of GABA analogs |
Apr, 2026
(1 year, 11 months from now) | |
US8795725 | AZURITY | GABA analog prodrug sustained release oral dosage forms |
Jun, 2029
(5 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
Orphan Drug Exclusivity(ODE) | Jun 06, 2019 |
Orphan Drug Exclusivity(ODE-25) | Jun 06, 2019 |
New Chemical Entity Exclusivity(NCE) | Apr 06, 2016 |
New Indication(I-652) | Jun 06, 2015 |
Drugs and Companies using GABAPENTIN ENACARBIL ingredient
NCE-1 date: 07 April, 2015
Market Authorisation Date: 13 December, 2011
Treatment: Management of postherpetic neuralgia (phn) in adults; Treatment of moderate-to-severe primary restless leg syndrome in adults
Dosage: TABLET, EXTENDED RELEASE;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11701326 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US11364230 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US10959991 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US11484498 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US10894039 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US11471409 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US10952998 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US10695329 | AZURITY | Amlodipine formulations |
Oct, 2037
(13 years from now) | |
US10799453 | AZURITY | Amlodipine formulations |
Apr, 2039
(14 years from now) |
Drugs and Companies using AMLODIPINE BENZOATE ingredient
Market Authorisation Date: 08 July, 2019
Treatment: Angina; Method of treating hypertension; A method of treating hypertension
Dosage: SUSPENSION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10751333 | AZURITY | Compositions and kits for omeprazole suspension |
Jul, 2039
(15 years from now) | |
US11103492 | AZURITY | Compositions and kits for omeprazole suspension |
Jul, 2039
(15 years from now) | |
US11633478 | AZURITY | Compositions and kits for Omeprazole suspension |
Jul, 2039
(15 years from now) | |
US11771686 | AZURITY | Compositions and kits for omeprazole suspension |
Mar, 2040
(15 years from now) |
Drugs and Companies using OMEPRAZOLE; SODIUM BICARBONATE ingredient
Market Authorisation Date: 30 August, 2022
Treatment: Short term treatment of active benign gastric ulcer
Dosage: FOR SUSPENSION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US7070581 | AZURITY | Dispenser for medicaments and method and apparatus for making same |
Jun, 2023
(9 months ago) | |
US8517997 | AZURITY | Dispenser for medicaments and method and apparatus for making same |
May, 2024
(24 days from now) | |
US10342787 | AZURITY | Non-aqueous liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US11806338 | AZURITY | Non-aqueous liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US11207306 | AZURITY | Non-aqueous liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US10576070 | AZURITY | Non-aqueous liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US11759457 | AZURITY | Liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US11517563 | AZURITY | Liquid nimodipine compositions |
Apr, 2038
(13 years from now) | |
US11413277 | AZURITY | Non-aqueous liquid nimodipine compositions |
Apr, 2038
(13 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
Orphan Drug Exclusivity(ODE-46) | May 10, 2020 |
Orphan Drug Exclusivity(ODE) | May 10, 2020 |
Drugs and Companies using NIMODIPINE ingredient
Market Authorisation Date: 10 May, 2013
Treatment: A method for the improvement of neurological outcome by reducing the incidence and severity of ischemic deficits in adult patients with subarachnoid hemorrhage (sah) from ruptured intracranial berry a...
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11771733 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US11179434 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US9814751 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US10940177 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US10039800 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US9616096 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US10265370 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US9463183 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) | |
US10406199 | AZURITY | Lisinopril formulations |
Nov, 2035
(11 years from now) |
Drugs and Companies using LISINOPRIL ingredient
Market Authorisation Date: 29 July, 2016
Treatment: Method of treating hypertension; Method of treatment of heart failure; Acute myocardial infarction
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11013703 | AZURITY | Sotalol compositions and uses of the same |
Apr, 2034
(9 years from now) | |
US10206895 | AZURITY | Sotalol compositions and uses of the same |
Apr, 2034
(9 years from now) | |
US11850222 | AZURITY | Sotalol compositions and uses of the same |
Nov, 2034
(10 years from now) | |
US9724297 | AZURITY | Sotalol compositions and uses of the same |
Aug, 2035
(11 years from now) |
Drugs and Companies using SOTALOL HYDROCHLORIDE ingredient
Market Authorisation Date: 22 October, 2014
Treatment: Indicated for the treatment of ventricular arrhythmias, such as sustained ventricular tachycardia, that in the judgement of the physician are life-threatening; Sotylize is indicated for the maintenanc...
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US9050307 | AZURITY | Method for the preparation of a levothyroxine solution |
Aug, 2031
(7 years from now) |
Drugs and Companies using LEVOTHYROXINE SODIUM ingredient
Market Authorisation Date: 30 November, 2020
Treatment: NA
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10166181 | AZURITY | Slow release pharmaceutical composition made of microgranules |
Jun, 2029
(5 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
Orphan Drug Exclusivity(ODE-149) | Jun 29, 2024 |
Orphan Drug Exclusivity(ODE) | Jun 29, 2024 |
New Product(NP) | Jun 29, 2020 |
Drugs and Companies using TRIPTORELIN PAMOATE ingredient
Market Authorisation Date: 29 June, 2017
Treatment: NA
Dosage: FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US10610485 | AZURITY | Methotrexate composition |
Jan, 2033
(8 years from now) | |
US11116724 | AZURITY | Methotrexate composition |
Jan, 2033
(8 years from now) | |
US10231927 | AZURITY | Methotrexate composition |
Jan, 2033
(8 years from now) | |
US9855215 | AZURITY | Methotrexate composition |
Jan, 2033
(8 years from now) | |
US9259427 | AZURITY | Methotrexate composition |
Jan, 2033
(8 years from now) |
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
Orphan Drug Exclusivity(ODE-137) | Apr 25, 2024 |
Orphan Drug Exclusivity(ODE-138) | Apr 25, 2024 |
Orphan Drug Exclusivity(ODE) | Apr 25, 2024 |
Drugs and Companies using METHOTREXATE SODIUM ingredient
Market Authorisation Date: 25 April, 2017
Treatment: A method for treating acute lymphoblastic leukemia; Treatment of juvenile rheumatoid arthritis
Dosage: SOLUTION;ORAL
Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US11478456 | AZURITY | Oral pharmaceutical composition comprising Zonisamide and process of preparation thereof |
Aug, 2038
(14 years from now) | |
US11529333 | AZURITY | Oral pharmaceutical composition comprising zonisamide and process of preparation thereof |
Aug, 2038
(14 years from now) |
Drugs and Companies using ZONISAMIDE ingredient
Market Authorisation Date: 15 July, 2022
Treatment: A method of treating seizures
Dosage: SUSPENSION;ORAL