Megestrol Acetate
- Product NDC
- 63629-2219
- 11-digit product format
- 636292219
- Labeler code
- 63629
- Product ID
- 63629-2219_4eadac46-bbed-473e-82dd-3f8e12a7553a
- 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
- 0000-00-00
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2219-1 | 63629221901 | 250 TABLET in 1 BOTTLE (63629-2219-1) | 250 tablet | 2021-03-22 | 0000-00-00 | No | No | Current |