CEFDINIR
- Product NDC
- 72189-186
- 11-digit product format
- 721890186
- Labeler code
- 72189
- Product ID
- 72189-186_2c4ea169-07c6-6bde-e063-6394a90a0890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFDINIR
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065473
- Marketing category
- ANDA
- Marketing start
- 2021-04-12
- 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 |
|---|
| 72189-186-32 | 72189018632 | 60 mL in 1 BOTTLE (72189-186-32) | 60 ml | 2021-04-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| CEFDINIR | DIRECT RX | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 8 |