Cefdinir
- Product NDC
- 68071-5145
- 11-digit product format
- 680715145
- Labeler code
- 68071
- Product ID
- 68071-5145_45120ef3-e746-6c39-e063-6394a90ad638
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2008-01-07
- Substance
- CEFDINIR
- Active strength
- 300 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| CI0FAO63WC | CEFDINIR | 91832-40-5 | CEFDINIR |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-5145-2 | 68071514502 | 20 CAPSULE in 1 BOTTLE (68071-5145-2) | 20 capsule | 2020-01-08 | No | No | Historical |
| 68071-5145-7 | 68071514507 | 14 CAPSULE in 1 BOTTLE (68071-5145-7) | 14 capsule | 2025-12-03 | No | No | Historical |