Cefadroxil
- Product NDC
- 68788-0708
- 11-digit product format
- 687880708
- Labeler code
- 68788
- Product ID
- 68788-0708_0dd86da6-a4ed-41f5-8737-464c7762a17c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA065392
- Marketing category
- ANDA
- Marketing start
- 2014-10-20
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record