Progesterone
- Product NDC
- 17478-767
- 11-digit product format
- 174780767
- Labeler code
- 17478
- Product ID
- 17478-767_c041d019-ffab-4e30-a3d4-3ef61f4d15c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Akorn
- 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
- 2023-12-31
- 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 |
|---|
| 17478-767-10 | 17478076710 | 100 CAPSULE in 1 BOTTLE, PLASTIC (17478-767-10) | 100 capsule | 2012-10-04 | 0000-00-00 | No | No | Current |