Cefadroxil
- Product NDC
- 68289-014
- 11-digit product format
- 682890014
- Labeler code
- 68289
- Product ID
- 68289-014_f219e051-99c0-4142-8bd8-269b049e9722
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Jazeera Pharmaceutical
- Application
- ANDA091036
- Marketing category
- ANDA
- Marketing start
- 2012-11-28
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#