Cefdinir
- Product NDC
- 68071-3806
- 11-digit product format
- 680713806
- Labeler code
- 68071
- Product ID
- 68071-3806_2fb43adf-3e71-176f-e063-6394a90a29e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA065259
- Marketing category
- ANDA
- Marketing start
- 2006-05-31
- Substance
- CEFDINIR
- Active strength
- 125 mg/5mL
- 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 |
|---|
| 68071-3806-1 | 68071380601 | 100 mL in 1 BOTTLE (68071-3806-1) | 100 ml | 2025-03-06 | No | No | Historical |