Progesterone
- Product NDC
- 0093-5353
- 11-digit product format
- 000935353
- Labeler code
- 0093
- Product ID
- 0093-5353_f6652397-fe7e-475f-9aff-954a779ee207
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA202121
- Marketing category
- ANDA
- Marketing start
- 2012-03-01
- Marketing end
- 2020-05-31
- Substance
- PROGESTERONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record