Mafenide Acetate
- Product NDC
- 50742-310
- 11-digit product format
- 507420310
- Labeler code
- 50742
- Product ID
- 50742-310_1fcf6a45-6ee9-4a3a-b8d8-0b00cbef3d6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mafenide Acetate
- Dosage form
- POWDER, FOR SOLUTION
- Route
- TOPICAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA206716
- Marketing category
- ANDA
- Marketing start
- 2018-10-22
- Marketing end
- 0000-00-00
- Substance
- MAFENIDE ACETATE
- Active strength
- 50 g/1
- Pharmacologic classes
- Methylated Sulfonamide Antibacterial [EPC],Methylated Sulfonamides [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-310-25 | 50742031025 | 5 PACKET in 1 CARTON (50742-310-25) > 1 POWDER, FOR SOLUTION in 1 PACKET (50742-310-50) | 5 packet | 2018-10-22 | 0000-00-00 | No | No | Current |