Megestrol Acetate
- Product NDC
- 0121-0887
- 11-digit product format
- 001210887
- Labeler code
- 0121
- Product ID
- 0121-0887_a1253cdc-ddc8-2d31-e053-2995a90adfe6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA204688
- Marketing category
- ANDA
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- MEGESTROL ACETATE
- Active strength
- 625 mg/5mL
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0887-20 | 00121088720 | 2 CASE in 1 CASE (0121-0887-20) > 4 TRAY in 1 CASE (0121-0887-40) > 10 CUP, UNIT-DOSE in 1 TRAY (0121-0887-05) > 5 mL in 1 CUP, UNIT-DOSE | 2 case | 2020-03-18 | 0000-00-00 | No | No | Current |