Progesterone
- Product NDC
- 71335-0713
- 11-digit product format
- 713350713
- Labeler code
- 71335
- Product ID
- 71335-0713_644f433e-ca59-45be-a67e-9cd416c85100
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202121
- Marketing category
- ANDA
- Marketing start
- 2012-03-01
- Marketing end
- 0000-00-00
- Substance
- PROGESTERONE
- Active strength
- 200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0713-1 | 71335071301 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0713-1) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 71335-0713-2 | 71335071302 | 28 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0713-2) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 71335-0713-3 | 71335071303 | 18 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0713-3) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 71335-0713-4 | 71335071304 | 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0713-4) | 2018-03-05 | 0000-00-00 | No | No | Current |
| 71335-0713-5 | 71335071305 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0713-5) | 2018-03-05 | 0000-00-00 | No | No | Current |