CEFACLOR
- Product NDC
- 50090-0518
- 11-digit product format
- 500900518
- Labeler code
- 50090
- Product ID
- 50090-0518_43003379-7b34-4a95-8409-2ca4ccd7833f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFACLOR
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065350
- Marketing category
- ANDA
- Marketing start
- 2007-05-01
- Marketing end
- 0000-00-00
- Substance
- CEFACLOR
- 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