Cephalexin
- Product NDC
- 70518-2077
- 11-digit product format
- 705182077
- Labeler code
- 70518
- Product ID
- 70518-2077_89099c08-fbaa-3c06-e053-2995a90a0331
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA062703
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record