cefuroxime axetil
- Product NDC
- 68788-9700
- 11-digit product format
- 687889700
- Labeler code
- 68788
- Product ID
- 68788-9700_369bde7a-952c-483c-a667-117ecd4d6153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefuroxime axetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA065135
- Marketing category
- ANDA
- Marketing start
- 2013-03-15
- Marketing end
- 0000-00-00
- Substance
- CEFUROXIME AXETIL
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record