Cefdinir
- Product NDC
- 68788-7062
- 11-digit product format
- 687887062
- Labeler code
- 68788
- Product ID
- 68788-7062_e328ed71-ad70-4c0c-b618-d15e4bbdd8fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA065259
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7062-1 | 68788706201 | 100 mL in 1 BOTTLE (68788-7062-1) | 100 ml | 2018-01-04 | 0000-00-00 | No | No | Current |