cephalexin
- Product NDC
- 70518-0912
- 11-digit product format
- 705180912
- Labeler code
- 70518
- Product ID
- 70518-0912_8f0b2faf-8f21-a8e5-e053-2995a90a520d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065248
- Marketing category
- ANDA
- Marketing start
- 2017-12-15
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record