Medroxyprogesterone Acetate
- Product NDC
- 70518-3070
- 11-digit product format
- 705183070
- Labeler code
- 70518
- Product ID
- 70518-3070_efb80511-4283-024c-e053-2a95a90af004
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Medroxyprogesterone Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040159
- Marketing category
- ANDA
- Marketing start
- 2021-04-10
- Marketing end
- 0000-00-00
- Substance
- MEDROXYPROGESTERONE ACETATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-3070-0 | 70518307000 | 30 TABLET in 1 BLISTER PACK (70518-3070-0) | 30 tablet | 2021-04-10 | 0000-00-00 | No | No | Current |
| 70518-3070-1 | 70518307001 | 30 TABLET in 1 BLISTER PACK (70518-3070-1) | 30 tablet | 2021-11-11 | 0000-00-00 | No | No | Current |