Megestrol Acetate
- Product NDC
- 63629-7631
- 11-digit product format
- 636297631
- Labeler code
- 63629
- Product ID
- 63629-7631_bc77caf7-031e-41af-a7a7-85068b121e5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072423
- Marketing category
- ANDA
- Marketing start
- 1988-08-08
- Marketing end
- 2024-12-31
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63629-7631-1 | 63629763101 | 30 TABLET in 1 BOTTLE (63629-7631-1) | 30 tablet | 2018-05-18 | 0000-00-00 | No | No | Current |
| 63629-7631-2 | 63629763102 | 100 TABLET in 1 BOTTLE (63629-7631-2) | 100 tablet | 2018-05-18 | 0000-00-00 | No | No | Current |
| 63629-7631-3 | 63629763103 | 15 TABLET in 1 BOTTLE (63629-7631-3) | 15 tablet | 2021-03-04 | 0000-00-00 | No | No | Current |