Megestrol Acetate
- Product NDC
- 49884-289
- 11-digit product format
- 498840289
- Labeler code
- 49884
- Product ID
- 49884-289_8707d220-fcf6-4b48-ae5f-1fdb44addcb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA072422
- Marketing category
- ANDA
- Marketing start
- 1988-08-08
- Marketing end
- 2024-08-31
- Substance
- MEGESTROL ACETATE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-289-01 | 49884028901 | 100 TABLET in 1 BOTTLE (49884-289-01) | 100 tablet | 1988-08-08 | 0000-00-00 | No | No | Current |