FDA Orange Book · active-ingredient family
Estradiol cypionate
Estradiol cypionate is approved in 2 FDA applications, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
0
Brand (NDA)
2
Generics (ANDA)
0
Listed patents
0
Exclusivity periods
Generic (ANDA) products (2)
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| DEPO-ESTRADIOL×3 | PFIZER | ANDA 085470 | — | Approved Prior to Jan 1, 1982 | |
| ESTRADIOL CYPIONATE | DR REDDYS | ANDA 085620 | — | Approved Prior to Jan 1, 1982 |
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Estradiol cypionate — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.
