Cefadroxil
- Product NDC
- 68071-4550
- 11-digit product format
- 680714550
- Labeler code
- 68071
- Product ID
- 68071-4550_7535db78-b567-c847-e053-2a91aa0aad74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2007-01-25
- 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