Megestrol Acetate
- Product NDC
- 51079-434
- 11-digit product format
- 510790434
- Labeler code
- 51079
- Product ID
- 51079-434_96b16cf3-dfbf-9968-e053-2995a90a3b9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA074621
- Marketing category
- ANDA
- Marketing start
- 1997-08-07
- Marketing end
- 2021-03-31
- 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 |
|---|
| 51079-434-20 | 51079043420 | 100 BLISTER PACK in 1 CARTON (51079-434-20) > 1 TABLET in 1 BLISTER PACK (51079-434-01) | 100 blister pack | 1997-08-07 | 2021-03-31 | No | No | Current |