PROGESTERONE
- Product NDC
- 72189-347
- 11-digit product format
- 721890347
- Labeler code
- 72189
- Product ID
- 72189-347_2c4c6aca-4b89-7f9f-e063-6394a90a0a23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA205229
- Marketing category
- ANDA
- Marketing start
- 2022-04-14
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS], Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4G7DS2Q64Y | PROGESTERONE | 57-83-0 | PROGESTERONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-347-90 | 72189034790 | 90 CAPSULE in 1 BOTTLE (72189-347-90) | 90 capsule | 2022-04-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PROGESTERONE | Direct Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 3 |