Cefdinir
- Product NDC
- 68071-2503
- 11-digit product format
- 680712503
- Labeler code
- 68071
- Product ID
- 68071-2503_2badf51d-00cc-a56f-e063-6394a90a004d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210220
- Marketing category
- ANDA
- Marketing start
- 2021-02-20
- 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 |
|---|
| 68071-2503-2 | 68071250302 | 20 CAPSULE in 1 BOTTLE (68071-2503-2) | 20 capsule | 2021-02-20 | No | No | Historical |
| 68071-2503-3 | 68071250303 | 30 CAPSULE in 1 BOTTLE (68071-2503-3) | 30 capsule | 2025-01-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Cefdinir | NuCare Pharmaceuticals,Inc. | 2025-01-14 | HUMAN PRESCRIPTION DRUG LABEL | 3 |