Mafenide acetate
- Product NDC
- 49884-902
- 11-digit product format
- 498840902
- Labeler code
- 49884
- Product ID
- 49884-902_2ac267d5-35a9-4310-be5b-97b5dd6c46cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mafenide acetate
- Dosage form
- POWDER, FOR SOLUTION
- Route
- TOPICAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA201511
- Marketing category
- ANDA
- Marketing start
- 2013-02-12
- 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
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49884-902 | MAFENIDE ACETATE POWDER, FOR SOLUTION [PAR PHARMACEUTICAL, INC.] | 16 | Legacy NDC | 20231123_e48cc935-2058-48c0-9281-b8b919629493.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-902-52 | 49884090252 | 1 CARTON in 1 PACKET (49884-902-52) > 5 POWDER, FOR SOLUTION in 1 CARTON (49884-902-78) | 1 carton | 2013-02-12 | 0000-00-00 | No | No | Current |