Megestrol Acetate
- Product NDC
- 0121-4776
- 11-digit product format
- 001214776
- Labeler code
- 0121
- Product ID
- 0121-4776_ee9c9ed1-d2a8-09d8-e053-2995a90a39c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MEGESTROL ACETATE
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA076721
- Marketing category
- ANDA
- Marketing start
- 2006-07-07
- Marketing end
- 0000-00-00
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0121-4776-00 | 00121477600 | 10 TRAY in 1 CASE (0121-4776-00) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-4776-10) | 10 tray | 2006-07-07 | 0000-00-00 | No | No | Current |
| 0121-4776-10 | 00121477610 | 10 mL in 1 CUP, UNIT-DOSE (0121-4776-10) | 10 ml | 2006-07-07 | 2023-04-28 | No | No | Current |
| 0121-4776-40 | 00121477640 | 4 TRAY in 1 CASE (0121-4776-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-4776-10) | 4 tray | 2006-07-07 | 0000-00-00 | No | No | Current |