Cefdinir
- Product NDC
- 68788-7478
- 11-digit product format
- 687887478
- Labeler code
- 68788
- Product ID
- 68788-7478_f77124a1-7e0f-4d1e-aea6-f4e0e47b5dd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065473
- Marketing category
- ANDA
- Marketing start
- 2020-04-13
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7478-6 | 68788747806 | 1 BOTTLE in 1 CARTON (68788-7478-6) > 60 mL in 1 BOTTLE | 1 bottle | 2020-04-13 | 0000-00-00 | No | No | Current |