Cefdinir
- Product NDC
- 68071-4792
- 11-digit product format
- 680714792
- Labeler code
- 68071
- Product ID
- 68071-4792_bb8e24ee-79e3-8c2c-e053-2a95a90a69e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065473
- Marketing category
- ANDA
- Marketing start
- 2007-12-14
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4792-6 | 68071479206 | 60 mL in 1 BOTTLE (68071-4792-6) | 60 ml | 2019-03-07 | 0000-00-00 | No | No | Current |