cephalexin
- Product NDC
- 70934-037
- 11-digit product format
- 709340037
- Labeler code
- 70934
- Product ID
- 70934-037_70a7e53f-1d9b-5ef6-e053-2991aa0a297d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065248
- Marketing category
- ANDA
- Marketing start
- 2017-10-31
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 250 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