FULVICIN P Drug Patent Profile
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When do Fulvicin P patents expire, and what generic alternatives are available?
Fulvicin P is a drug marketed by Chartwell Rx and is included in one NDA.
The generic ingredient in FULVICIN P is griseofulvin, ultramicrosize. There is one drug master file entry for this compound. Eight suppliers are listed for this compound. Additional details are available on the griseofulvin, ultramicrosize profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Fulvicin P
A generic version of FULVICIN P was approved as griseofulvin, ultramicrosize by MOUNTAIN on January 9th, 2014.
AI Deep Research
Questions you can ask:
- What is the 5 year forecast for FULVICIN P?
- What are the global sales for FULVICIN P?
- What is Average Wholesale Price for FULVICIN P?
Summary for FULVICIN P
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| DailyMed Link: | FULVICIN P at DailyMed |
US Patents and Regulatory Information for FULVICIN P
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chartwell Rx | FULVICIN P/G | griseofulvin, ultramicrosize | TABLET;ORAL | 061996-001 | Approved Prior to Jan 1, 1982 | AB | RX | No | No | ⤷ Get Started Free | ⤷ Get Started Free | ⤷ Get Started Free | |||
| Chartwell Rx | FULVICIN P/G 330 | griseofulvin, ultramicrosize | TABLET;ORAL | 061996-004 | Apr 6, 1982 | RX | No | No | ⤷ Get Started Free | ⤷ Get Started Free | ⤷ Get Started Free | ||||
| Chartwell Rx | FULVICIN P/G | griseofulvin, ultramicrosize | TABLET;ORAL | 061996-002 | Approved Prior to Jan 1, 1982 | AB | RX | No | No | ⤷ Get Started Free | ⤷ Get Started Free | ⤷ Get Started Free | |||
| Chartwell Rx | FULVICIN P/G 165 | griseofulvin, ultramicrosize | TABLET;ORAL | 061996-003 | Apr 6, 1982 | RX | No | No | ⤷ Get Started Free | ⤷ Get Started Free | ⤷ Get Started Free | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
