Progesterone
- Product NDC
- 70518-3392
- 11-digit product format
- 705183392
- Labeler code
- 70518
- Product ID
- 70518-3392_da7eacd6-af1f-32c8-e053-2a95a90a459a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211285
- Marketing category
- ANDA
- Marketing start
- 2022-03-18
- 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 |
|---|
| 70518-3392-0 | 70518339200 | 100 POUCH in 1 BOX (70518-3392-0) > 1 CAPSULE in 1 POUCH (70518-3392-1) | 100 pouch | 2022-03-18 | 0000-00-00 | No | No | Current |