Megestrol Acetate
- Product NDC
- 49884-230
- 11-digit product format
- 498840230
- Labeler code
- 49884
- Product ID
- 49884-230_76074af3-4507-4a7a-abfd-27a3e4caef0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA021778
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-07-28
- Marketing end
- 2023-05-31
- Substance
- MEGESTROL ACETATE
- Active strength
- 125 mg/mL
- 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 |
|---|
| 49884-230-69 | 49884023069 | 150 mL in 1 BOTTLE (49884-230-69) | 150 ml | 2015-07-28 | 2023-05-31 | No | No | Current |