PROGESTERONE

Product NDC
68071-3529
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PROGESTERONE
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA200900
Marketing category
ANDA
Substance
PROGESTERONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3529-330 CAPSULE in 1 BOTTLE (68071-3529-3) 2023-11-28NoHistorical
68071-3529-660 CAPSULE in 1 BOTTLE (68071-3529-6) 2025-11-03NoHistorical
68071-3529-8180 CAPSULE in 1 BOTTLE (68071-3529-8) 2025-10-09NoHistorical
68071-3529-990 CAPSULE in 1 BOTTLE (68071-3529-9) 2023-11-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PROGESTERONE - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2025-11-03HUMAN PRESCRIPTION DRUG LABEL5
PROGESTERONE - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2025-02-03HUMAN PRESCRIPTION DRUG LABEL3