Cefadroxil
- Product NDC
- 49999-021
- 11-digit product format
- 499990021
- Labeler code
- 49999
- Product ID
- 49999-021_eaf9b4bf-aa93-417b-8d6e-d6e2e6fdde0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065311
- Marketing category
- ANDA
- Marketing start
- 2006-02-07
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record