Megestrol Acetate
- Product NDC
- 0904-7072
- 11-digit product format
- 009047072
- Labeler code
- 0904
- Product ID
- 0904-7072_4c3f5466-d935-4063-8dbc-14480d1a4187
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA075671
- Marketing category
- ANDA
- Marketing start
- 2001-07-25
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7072-18 | 00904707218 | 40 CUP, UNIT-DOSE in 1 CASE (0904-7072-18) > 10 mL in 1 CUP, UNIT-DOSE | 2001-07-25 | 0000-00-00 | No | No | Current |
| 0904-7072-72 | 00904707272 | 100 CUP, UNIT-DOSE in 1 CASE (0904-7072-72) > 10 mL in 1 CUP, UNIT-DOSE | 2001-07-25 | 0000-00-00 | No | No | Current |
| 0904-7072-95 | 00904707295 | 50 CUP, UNIT-DOSE in 1 CASE (0904-7072-95) > 10 mL in 1 CUP, UNIT-DOSE | 2001-07-25 | 0000-00-00 | No | No | Current |