Progesterone
- Product NDC
- 76420-072
- 11-digit product format
- 764200072
- Labeler code
- 76420
- Product ID
- 76420-072_ead2c72c-bda1-2f0c-e053-2995a90af3cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA211285
- Marketing category
- ANDA
- Marketing start
- 2018-10-26
- Substance
- PROGESTERONE
- Active strength
- 100 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 |
|---|
| 76420-072-10 | 76420007210 | 100 CAPSULE in 1 BOTTLE (76420-072-10) | 100 capsule | 2019-12-24 | No | No | Historical |
| 76420-072-30 | 76420007230 | 30 CAPSULE in 1 BOTTLE (76420-072-30) | 30 capsule | 2019-12-24 | No | No | Historical |
| 76420-072-90 | 76420007290 | 90 CAPSULE in 1 BOTTLE (76420-072-90) | 90 capsule | 2019-12-24 | No | No | Historical |