OLOPATADINE Drug Patent Profile
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When do Olopatadine patents expire, and what generic alternatives are available?
Olopatadine is a drug marketed by Alembic, Apotex, Barr Labs Inc, Bausch And Lomb Inc, Eugia Pharma, Fdc Ltd, Florida, Gland, Glenmark Pharms, Rising, Sciegen Pharms, Somerset, Somerset Theraps Llc, USV, Zambon Spa, Amneal, Apotex Inc, Hikma, and Padagis Israel. and is included in twenty-nine NDAs.
The generic ingredient in OLOPATADINE is olopatadine hydrochloride. There is one drug master file entry for this compound. Forty-nine suppliers are listed for this compound. Additional details are available on the olopatadine hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Olopatadine
A generic version of OLOPATADINE was approved as olopatadine hydrochloride by APOTEX INC on October 8th, 2014.
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Questions you can ask:
- What is the 5 year forecast for OLOPATADINE?
- What are the global sales for OLOPATADINE?
- What is Average Wholesale Price for OLOPATADINE?
Summary for OLOPATADINE
| US Patents: | 0 |
| Applicants: | 19 |
| NDAs: | 29 |
| Drug Prices: | Drug price information for OLOPATADINE |
| Drug Sales Revenues: | Drug sales revenues for OLOPATADINE |
| DailyMed Link: | OLOPATADINE at DailyMed |
US Patents and Regulatory Information for OLOPATADINE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hikma | OLOPATADINE HYDROCHLORIDE | olopatadine hydrochloride | SPRAY, METERED;NASAL | 213757-001 | Aug 19, 2020 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Padagis Israel | OLOPATADINE HYDROCHLORIDE | olopatadine hydrochloride | SPRAY, METERED;NASAL | 202853-001 | Jan 31, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Alembic | OLOPATADINE HYDROCHLORIDE | olopatadine hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 209919-001 | Dec 7, 2018 | OTC | 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 |
