Cefdinir
- Product NDC
- 68071-1788
- 11-digit product format
- 680711788
- Labeler code
- 68071
- Product ID
- 68071-1788_bb18e6d8-d992-60ca-e053-2a95a90ab663
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065332
- Marketing category
- ANDA
- Marketing start
- 2007-05-08
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR MONOHYDRATE
- Active strength
- 250 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 |
|---|
| 68071-1788-6 | 68071178806 | 60 mL in 1 BOTTLE (68071-1788-6) | 60 ml | 2018-11-09 | 0000-00-00 | No | No | Current |