Progesterone
- Product NDC
- 53002-1760
- 11-digit product format
- 530021760
- Labeler code
- 53002
- Product ID
- 53002-1760_e507bac9-3108-4c11-b20b-3fd3ce992e13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA200456
- Marketing category
- ANDA
- Marketing start
- 2012-10-04
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-1760-3 | 53002176003 | 30 CAPSULE in 1 BOTTLE (53002-1760-3) | 30 capsule | 2019-01-01 | 0000-00-00 | No | No | Current |