Cefdinir
- Product NDC
- 76420-328
- 11-digit product format
- 764200328
- Labeler code
- 76420
- Product ID
- 76420-328_331b63bf-fd36-155d-e063-6294a90aec23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA065259
- Marketing category
- ANDA
- Marketing start
- 2007-05-07
- Substance
- CEFDINIR
- Active strength
- 250 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 |
|---|
| 76420-328-01 | 76420032801 | 100 mL in 1 BOTTLE (76420-328-01) | 100 ml | 2025-04-19 | No | No | Historical |
| 76420-328-60 | 76420032860 | 60 mL in 1 BOTTLE (76420-328-60) | 60 ml | 2025-04-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Cefdinir for Oral Suspension USP | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |