Megestrol acetate
- Product NDC
- 51991-313
- 11-digit product format
- 519910313
- Labeler code
- 51991
- Product ID
- 51991-313_5f045c30-8e44-413b-8419-697e95d16623
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MEGESTROL ACETATE
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA204688
- Marketing category
- ANDA
- Marketing start
- 2017-12-01
- Marketing end
- 2022-07-31
- 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 |
|---|
| 51991-313-59 | 51991031359 | 150 mL in 1 BOTTLE (51991-313-59) | 150 ml | 2017-12-01 | 2022-07-31 | No | No | Current |