cefuroxime axetil
- Product NDC
- 57297-303
- 11-digit product format
- 572970303
- Labeler code
- 57297
- Product ID
- 57297-303_33afa15e-6c42-49e0-afc1-c3c5fb59e7ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefuroxime axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- LUPIN LIMITED
- Application
- ANDA065135
- Marketing category
- ANDA
- Marketing start
- 2003-07-25
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#