OLMESARTAN Drug Patent Profile
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When do Olmesartan patents expire, and when can generic versions of Olmesartan launch?
Olmesartan is a drug marketed by Accord Hlthcare, Alembic, Alkem Labs Ltd, Amneal, Aurobindo Pharma, Cadila Pharms Ltd, Chartwell Rx, Glenmark Pharms Ltd, Hetero Labs Ltd V, Inventia, Jubilant Generics, Lupin, Macleods Pharms Ltd, Micro Labs, MSN, Prinston Inc, Qilu, Rising, Sandoz, Sciegen Pharms, Sunshine, Teva Pharms Usa, Torrent, Umedica, Zydus Pharms, Hangzhou Binjiang, Natco Pharma Usa, Ph Health, and Piramal. and is included in forty-eight NDAs.
The generic ingredient in OLMESARTAN is amlodipine besylate; hydrochlorothiazide; olmesartan medoxomil. There are fifty drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the amlodipine besylate; hydrochlorothiazide; olmesartan medoxomil profile page.
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Summary for OLMESARTAN
| US Patents: | 0 |
| Applicants: | 29 |
| NDAs: | 48 |
| Drug Prices: | Drug price information for OLMESARTAN |
| DailyMed Link: | OLMESARTAN at DailyMed |
US Patents and Regulatory Information for OLMESARTAN
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Umedica | OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 207135-003 | Jul 18, 2019 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Msn | OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; olmesartan medoxomil | TABLET;ORAL | 217398-002 | Sep 26, 2025 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Micro Labs | OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 206372-002 | Sep 17, 2019 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Jubilant Generics | OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 205482-002 | Apr 24, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |


