VALPROIC Drug Patent Profile
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Which patents cover Valproic, and when can generic versions of Valproic launch?
Valproic is a drug marketed by Bionpharma, Catalent, Chartwell Rx, Hibrow Hlthcare, Par Pharm, Scherer Rp, Sun Pharm Inds Ltd, Ani Pharms, Hikma, Lannett Co Inc, Pai Holdings, Pharm Assoc, Pharmobedient Cnsltg, and Quagen. and is included in fifteen NDAs.
The generic ingredient in VALPROIC is valproic acid. There are seventeen drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the valproic acid profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Valproic
A generic version of VALPROIC was approved as valproic acid by CATALENT on October 29th, 1991.
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Questions you can ask:
- What is the 5 year forecast for VALPROIC?
- What are the global sales for VALPROIC?
- What is Average Wholesale Price for VALPROIC?
Summary for VALPROIC
| US Patents: | 0 |
| Applicants: | 14 |
| NDAs: | 15 |
| Drug Prices: | Drug price information for VALPROIC |
| DailyMed Link: | VALPROIC at DailyMed |
US Patents and Regulatory Information for VALPROIC
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Bionpharma | VALPROIC ACID | valproic acid | CAPSULE;ORAL | 073484-001 | Jun 29, 1993 | AB | RX | No | Yes | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Sun Pharm Inds Ltd | VALPROIC ACID | valproic acid | CAPSULE;ORAL | 091037-001 | Feb 22, 2013 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Hibrow Hlthcare | VALPROIC ACID | valproic acid | CAPSULE;ORAL | 207611-001 | Aug 5, 2019 | DISCN | 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 |


