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). | ||||
US5856355 (Pediatric) | KARO HLTHCARE | Pharmaceutical composition |
Nov, 2012
(11 years ago) | |
US5681849 | KARO HLTHCARE | Pharmaceutical composition for topical applications |
Oct, 2014
(9 years ago) | |
US5681849 (Pediatric) | KARO HLTHCARE | Pharmaceutical composition for topical applications |
Apr, 2015
(9 years ago) |
Lamisil At is owned by Karo Hlthcare.
Lamisil At contains Terbinafine.
Lamisil At has a total of 3 drug patents out of which 3 drug patents have expired.
Expired drug patents of Lamisil At are:
Lamisil At was authorised for market use on 24 July, 2006.
Lamisil At is available in gel;topical dosage forms.
The generics of Lamisil At are possible to be released after 28 April, 2015.
Drugs and Companies using TERBINAFINE ingredient
Market Authorisation Date: 24 July, 2006
Treatment: NA
Dosage: GEL;TOPICAL
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). | ||||
US5681849 | KARO HLTHCARE | Pharmaceutical composition for topical applications |
Oct, 2014
(9 years ago) | |
US5681849 (Pediatric) | KARO HLTHCARE | Pharmaceutical composition for topical applications |
Apr, 2015
(9 years ago) |
Lamisil At is owned by Karo Hlthcare.
Lamisil At contains Terbinafine Hydrochloride.
Lamisil At has a total of 2 drug patents out of which 2 drug patents have expired.
Expired drug patents of Lamisil At are:
Lamisil At was authorised for market use on 17 March, 2000.
Lamisil At is available in solution;topical dosage forms.
The generics of Lamisil At are possible to be released after 28 April, 2015.
Drugs and Companies using TERBINAFINE HYDROCHLORIDE ingredient
Market Authorisation Date: 17 March, 2000
Treatment: NA
Dosage: SOLUTION;TOPICAL