Cefdinir
- Product NDC
- 68788-9760
- 11-digit product format
- 687889760
- Labeler code
- 68788
- Product ID
- 68788-9760_040791c2-f00a-4aa5-b423-1332210b447e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065418
- Marketing category
- ANDA
- Marketing start
- 2015-08-20
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR MONOHYDRATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record