Megestrol Acetate
- Product NDC
- 55154-5776
- 11-digit product format
- 551545776
- Labeler code
- 55154
- Product ID
- 55154-5776_41a5da12-db71-445b-a90e-a56961ae5e5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MEGESTROL ACETATE
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA076721
- Marketing category
- ANDA
- Marketing start
- 2006-07-07
- Marketing end
- 2023-01-31
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-5776-5 | 55154577605 | 5 CUP, UNIT-DOSE in 1 BAG (55154-5776-5) > 10 mL in 1 CUP, UNIT-DOSE | 2006-07-07 | 2023-01-31 | No | No | Current |