VICODIN Drug Patent Profile
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Which patents cover Vicodin, and what generic alternatives are available?
Vicodin is a drug marketed by Abbott and Abbvie and is included in four NDAs.
The generic ingredient in VICODIN is acetaminophen; hydrocodone bitartrate. There are sixty-six drug master file entries for this compound. Forty-one suppliers are listed for this compound. Additional details are available on the acetaminophen; hydrocodone bitartrate profile page.
Summary for VICODIN
US Patents: | 0 |
Applicants: | 2 |
NDAs: | 4 |
Raw Ingredient (Bulk) Api Vendors: | 182 |
Clinical Trials: | 37 |
Patent Applications: | 4,117 |
Formulation / Manufacturing: | see details |
Drug Prices: | Drug price information for VICODIN |
DailyMed Link: | VICODIN at DailyMed |
Recent Clinical Trials for VICODIN
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Weill Medical College of Cornell University | Phase 4 |
Boston University | Phase 4 |
Antonios Likourezos | Phase 4 |
Anatomical Therapeutic Chemical (ATC) Classes for VICODIN
US Patents and Regulatory Information for VICODIN
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Abbott | VICODIN | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 085667-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Abbvie | VICODIN HP | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 040117-001 | Sep 23, 1996 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Abbvie | VICODIN | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 088058-001 | Jan 7, 1983 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Abbvie | VICODIN ES | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 089736-001 | Dec 9, 1988 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |