Prometrium
- Product NDC
- 69543-372
- 11-digit product format
- 695430372
- Labeler code
- 69543
- Product ID
- 69543-372_5ddff444-38c1-455f-a911-bd5d31f56275
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- NDA019781
- Marketing category
- NDA
- Marketing start
- 2016-07-15
- 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
- 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 |
|---|
| 69543-372-10 | 69543037210 | 100 CAPSULE in 1 BOTTLE (69543-372-10) | 100 capsule | 2016-07-15 | 2023-08-31 | No | No | Current |
| 69543-372-30 | 69543037230 | 30 CAPSULE in 1 BOTTLE (69543-372-30) | 30 capsule | 2021-06-01 | 0000-00-00 | No | No | Current |