Megestrol Acetate
- Product NDC
- 0904-3571
- 11-digit product format
- 009043571
- Labeler code
- 0904
- Product ID
- 0904-3571_5f559a52-e6fc-4df3-a774-cd28a8bc64dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA072423
- Marketing category
- ANDA
- Marketing start
- 2004-02-16
- Marketing end
- 2023-07-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-3571-61 | 00904357161 | 100 BLISTER PACK in 1 CARTON (0904-3571-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2004-02-16 | 2023-07-31 | No | No | Current |