Progesterone
- Product NDC
- 68788-7199
- 11-digit product format
- 687887199
- Labeler code
- 68788
- Product ID
- 68788-7199_d1ccb4b3-b75e-4a7c-b5e8-2c93b8be4192
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA200456
- Marketing category
- ANDA
- Marketing start
- 2018-07-19
- Marketing end
- 0000-00-00
- Substance
- PROGESTERONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7199-3 | 68788719903 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-7199-3) | 30 capsule | 2018-07-19 | 0000-00-00 | No | No | Current |
| 68788-7199-6 | 68788719906 | 60 CAPSULE in 1 BOTTLE, PLASTIC (68788-7199-6) | 60 capsule | 2018-07-19 | 0000-00-00 | No | No | Current |
| 68788-7199-9 | 68788719909 | 90 CAPSULE in 1 BOTTLE, PLASTIC (68788-7199-9) | 90 capsule | 2018-07-19 | 0000-00-00 | No | No | Current |