Cephalexin
- Product NDC
- 50090-2552
- 11-digit product format
- 500902552
- Labeler code
- 50090
- Product ID
- 50090-2552_fd5a02c1-e7aa-47c5-80c6-5ef6f9a56439
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2007-04-12
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record