DEPO-ESTRADIOL Drug Patent Profile
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When do Depo-estradiol patents expire, and what generic alternatives are available?
Depo-estradiol is a drug marketed by Pfizer and is included in one NDA.
The generic ingredient in DEPO-ESTRADIOL is estradiol cypionate. There are seventy-five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the estradiol cypionate profile page.
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Questions you can ask:
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Summary for DEPO-ESTRADIOL
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 1 |
Finished Product Suppliers / Packagers: | 1 |
Raw Ingredient (Bulk) Api Vendors: | 62 |
Clinical Trials: | 1,002 |
Patent Applications: | 1,580 |
Drug Prices: | Drug price information for DEPO-ESTRADIOL |
DailyMed Link: | DEPO-ESTRADIOL at DailyMed |
Recent Clinical Trials for DEPO-ESTRADIOL
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Anna Stanhewicz, PhD | Early Phase 1 |
McGill University Health Centre/Research Institute of the McGill University Health Centre | Phase 4 |
Alexion Pharmaceuticals, Inc. | Phase 1 |
Pharmacology for DEPO-ESTRADIOL
Drug Class | Estrogen |
Mechanism of Action | Estrogen Receptor Agonists |
US Patents and Regulatory Information for DEPO-ESTRADIOL
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Pfizer | DEPO-ESTRADIOL | estradiol cypionate | INJECTABLE;INJECTION | 085470-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Pfizer | DEPO-ESTRADIOL | estradiol cypionate | INJECTABLE;INJECTION | 085470-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Pfizer | DEPO-ESTRADIOL | estradiol cypionate | INJECTABLE;INJECTION | 085470-003 | Approved Prior to Jan 1, 1982 | RX | No | Yes | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |