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. | ||||
US4939130 | NOVARTIS | Substituted alkanediphosphonic acids and pharmaceutical use |
Sep, 2012
(11 years ago) | |
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US4939130 (Pediatric) | NOVARTIS | Substituted alkanediphosphonic acids and pharmaceutical use |
Mar, 2013
(11 years ago) | |
US8324189 | NOVARTIS | Use of zolendronate for the manufacture of a medicament for the treatment of bone metabolism diseases |
May, 2025
(1 year, 1 month from now) | |
US8324189 (Pediatric) | NOVARTIS | Use of zolendronate for the manufacture of a medicament for the treatment of bone metabolism diseases |
Nov, 2025
(1 year, 7 months from now) | |
US7932241 | NOVARTIS | Pharmaceutical products comprising bisphosphonates |
Feb, 2028
(3 years from now) |
Zometa is owned by Novartis.
Zometa contains Zoledronic Acid.
Zometa has a total of 5 drug patents out of which 2 drug patents have expired.
Expired drug patents of Zometa are:
Zometa was authorised for market use on 20 August, 2001.
Zometa is available in injectable;intravenous dosage forms.
Zometa can be used as hypercalcemia of malignancy.
The generics of Zometa are possible to be released after 05 February, 2028.
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
Pediatric Exclusivity(PED) | Sep 20, 2011 |
Drugs and Companies using ZOLEDRONIC ACID ingredient
Market Authorisation Date: 20 August, 2001
Treatment: Hypercalcemia of malignancy
Dosage: INJECTABLE;INTRAVENOUS