Cefdinir
- Product NDC
- 50090-1031
- 11-digit product format
- 500901031
- Labeler code
- 50090
- Product ID
- 50090-1031_cb8999c0-1c8e-48f8-ac2d-5e7773e2cb15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2008-01-07
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 300 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1031-1 | 50090103101 | 20 CAPSULE in 1 BOTTLE (50090-1031-1) | 20 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1031-2 | 50090103102 | 14 CAPSULE in 1 BOTTLE (50090-1031-2) | 14 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |