Cefdinir
- Product NDC
- 0781-6077
- 11-digit product format
- 007816077
- Labeler code
- 0781
- Product ID
- 0781-6077_990055e8-68da-4714-8a9b-02fbb244b570
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA065337
- Marketing category
- ANDA
- Marketing start
- 2007-04-06
- 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
- 2021-12-31
- 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 |
|---|
| 0781-6077-46 | 00781607746 | 100 mL in 1 BOTTLE (0781-6077-46) | 100 ml | 2007-04-06 | 0000-00-00 | No | No | Current |
| 0781-6077-61 | 00781607761 | 60 mL in 1 BOTTLE (0781-6077-61) | 60 ml | 2007-04-06 | 0000-00-00 | No | No | Current |