Cefdinir
- Product NDC
- 50090-1028
- 11-digit product format
- 500901028
- Labeler code
- 50090
- Product ID
- 50090-1028_82f0fc9f-e253-4740-a45d-a1ade5d2729d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefdinir
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065332
- Marketing category
- ANDA
- Marketing start
- 2007-05-08
- Marketing end
- 0000-00-00
- Substance
- CEFDINIR MONOHYDRATE
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#