AMCINONIDE Drug Patent Profile
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When do Amcinonide patents expire, and what generic alternatives are available?
Amcinonide is a drug marketed by Genus Lifesciences, Taro Pharm Inds, and Genus. and is included in five NDAs.
The generic ingredient in AMCINONIDE is amcinonide. There are three drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the amcinonide profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Amcinonide
A generic version of AMCINONIDE was approved as amcinonide by TARO PHARM INDS on May 31st, 2002.
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Questions you can ask:
- What is the 5 year forecast for AMCINONIDE?
- What are the global sales for AMCINONIDE?
- What is Average Wholesale Price for AMCINONIDE?
Summary for AMCINONIDE
US Patents: | 0 |
Applicants: | 3 |
NDAs: | 5 |
Finished Product Suppliers / Packagers: | 4 |
Raw Ingredient (Bulk) Api Vendors: | 53 |
Patent Applications: | 5,768 |
Drug Prices: | Drug price information for AMCINONIDE |
DailyMed Link: | AMCINONIDE at DailyMed |
Pharmacology for AMCINONIDE
Drug Class | Corticosteroid |
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Anatomical Therapeutic Chemical (ATC) Classes for AMCINONIDE
US Patents and Regulatory Information for AMCINONIDE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Genus Lifesciences | AMCINONIDE | amcinonide | CREAM;TOPICAL | 076065-001 | May 15, 2003 | AB | RX | No | Yes | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
Genus | AMCINONIDE | amcinonide | OINTMENT;TOPICAL | 076096-001 | Nov 19, 2002 | AB | RX | No | Yes | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
Taro Pharm Inds | AMCINONIDE | amcinonide | CREAM;TOPICAL | 076229-001 | May 31, 2002 | AB | RX | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | |||
Genus | AMCINONIDE | amcinonide | LOTION;TOPICAL | 076329-001 | Nov 6, 2002 | RX | No | Yes | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |