PROGESTERONE
- Product NDC
- 68788-8719
- 11-digit product format
- 687888719
- Labeler code
- 68788
- Product ID
- 68788-8719_669c35d3-43cd-48b6-b450-42fe5717f04b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA200900
- Marketing category
- ANDA
- Marketing start
- 2024-07-26
- 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 |
|---|
| 68788-8719-3 | 68788871903 | 30 CAPSULE in 1 BOTTLE (68788-8719-3) | 30 capsule | 2024-07-26 | No | No | Historical |