LOESTRIN Drug Patent Profile
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Which patents cover Loestrin, and when can generic versions of Loestrin launch?
Loestrin is a drug marketed by Teva Branded Pharm and is included in five NDAs.
The generic ingredient in LOESTRIN is ethinyl estradiol; norethindrone acetate. There are twenty-six drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; norethindrone acetate profile page.
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Summary for LOESTRIN
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 5 |
| Drug Prices: | Drug price information for LOESTRIN |
| DailyMed Link: | LOESTRIN at DailyMed |
US Patents and Regulatory Information for LOESTRIN
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Teva Branded Pharm | LOESTRIN 21 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 017875-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Teva Branded Pharm | LOESTRIN FE 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 017355-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Teva Branded Pharm | LOESTRIN 21 1/20 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 017876-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Teva Branded Pharm | LOESTRIN 24 FE | ethinyl estradiol; norethindrone acetate | TABLET;ORAL | 021871-001 | Feb 17, 2006 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Teva Branded Pharm | LOESTRIN FE 1/20 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-28 | 017354-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | 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 |
