GRISEOFULVIN,ULTRAMICROSIZE Drug Patent Profile
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Which patents cover Griseofulvin,ultramicrosize, and what generic alternatives are available?
Griseofulvin,ultramicrosize is a drug marketed by Sigmapharm Labs Llc and is included in one NDA.
The generic ingredient in GRISEOFULVIN,ULTRAMICROSIZE is griseofulvin, ultramicrosize. There is one drug master file entry for this compound. Five suppliers are listed for this compound. Additional details are available on the griseofulvin, ultramicrosize profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Griseofulvin,ultramicrosize
A generic version of GRISEOFULVIN,ULTRAMICROSIZE was approved as griseofulvin, ultramicrosize by MOUNTAIN on January 9th, 2014.
Summary for GRISEOFULVIN,ULTRAMICROSIZE
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Finished Product Suppliers / Packagers: | 1 |
| Formulation / Manufacturing: | see details |
| Drug Prices: | Drug price information for GRISEOFULVIN,ULTRAMICROSIZE |
| DailyMed Link: | GRISEOFULVIN,ULTRAMICROSIZE at DailyMed |
Pharmacology for GRISEOFULVIN,ULTRAMICROSIZE
| Drug Class | Tubulin Inhibiting Agent |
| Physiological Effect | Decreased Mitosis Microtubule Inhibition |
Anatomical Therapeutic Chemical (ATC) Classes for GRISEOFULVIN,ULTRAMICROSIZE
US Patents and Regulatory Information for GRISEOFULVIN,ULTRAMICROSIZE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Sigmapharm Labs Llc | GRISEOFULVIN,ULTRAMICROSIZE | griseofulvin, ultramicrosize | TABLET;ORAL | 202545-001 | Oct 22, 2012 | AB | RX | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | |||
| Sigmapharm Labs Llc | GRISEOFULVIN,ULTRAMICROSIZE | griseofulvin, ultramicrosize | TABLET;ORAL | 202545-002 | Oct 22, 2012 | AB | RX | 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 |
