Cefdinir
- Product NDC
- 68788-7606
- 11-digit product format
- 687887606
- Labeler code
- 68788
- Product ID
- 68788-7606_167ca2d5-5eeb-4444-ac18-bd1b8e322b9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065434
- Marketing category
- ANDA
- Marketing start
- 2020-02-06
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR
- Active strength
- 300 mg/1
- 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 |
|---|
| 68788-7606-2 | 68788760602 | 20 CAPSULE in 1 BOTTLE (68788-7606-2) | 20 capsule | 2020-02-06 | 0000-00-00 | No | No | Current |