Megestrol Acetate
- Product NDC
- 66689-020
- 11-digit product format
- 666890020
- Labeler code
- 66689
- Product ID
- 66689-020_5824a840-d3bb-4543-82d3-926b2903465f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- VistaPharm, Inc.
- Application
- ANDA075671
- Marketing category
- ANDA
- Marketing start
- 2012-08-22
- 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
- 2022-12-31
- 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 |
|---|
| 66689-020-50 | 66689002050 | 5 TRAY in 1 CASE (66689-020-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-020-01) | 5 tray | 2012-08-22 | 0000-00-00 | No | No | Current |
| 66689-020-99 | 66689002099 | 10 TRAY in 1 CASE (66689-020-99) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-020-01) | 10 tray | 2012-08-22 | 0000-00-00 | No | No | Current |