MICROGESTIN Drug Patent Profile
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Which patents cover Microgestin, and what generic alternatives are available?
Microgestin is a drug marketed by Dr Reddys Labs Sa and is included in two NDAs.
The generic ingredient in MICROGESTIN is ethinyl estradiol; norethindrone acetate. There are twenty-six drug master file entries for this compound. Twenty-six suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; norethindrone acetate profile page.
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Questions you can ask:
- What is the 5 year forecast for MICROGESTIN?
- What are the global sales for MICROGESTIN?
- What is Average Wholesale Price for MICROGESTIN?
Summary for MICROGESTIN
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 2 |
| Drug Prices: | Drug price information for MICROGESTIN |
| Drug Sales Revenues: | Drug sales revenues for MICROGESTIN |
| DailyMed Link: | MICROGESTIN at DailyMed |
US Patents and Regulatory Information for MICROGESTIN
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Dr Reddys Labs Sa | MICROGESTIN 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 075548-002 | Jul 30, 2003 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Dr Reddys Labs Sa | MICROGESTIN FE 1/20 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-28 | 075647-001 | Feb 5, 2001 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Dr Reddys Labs Sa | MICROGESTIN 1/20 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 075647-002 | Jul 30, 2003 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Dr Reddys Labs Sa | MICROGESTIN FE 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-28 | 075548-001 | Feb 5, 2001 | 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 |
