Megestrol Acetate
- Product NDC
- 71335-2181
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072423
- Marketing category
- ANDA
- Substance
- MEGESTROL ACETATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2181-1 | 30 TABLET in 1 BOTTLE (71335-2181-1) | 2022-10-25 | | No | Historical |
| 71335-2181-2 | 100 TABLET in 1 BOTTLE (71335-2181-2) | 2022-10-25 | | No | Historical |
| 71335-2181-3 | 15 TABLET in 1 BOTTLE (71335-2181-3) | 2022-10-25 | | No | Historical |