Cefdinir
- Product NDC
- 68071-3032
- 11-digit product format
- 680713032
- Labeler code
- 68071
- Product ID
- 68071-3032_a4ed9cf7-1567-089e-e053-2a95a90a6424
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA065418
- Marketing category
- ANDA
- Marketing start
- 2014-07-04
- Marketing end
- 2020-12-31
- Substance
- CEFDINIR MONOHYDRATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record