Cephalexin
- Product NDC
- 68788-7391
- 11-digit product format
- 687887391
- Labeler code
- 68788
- Product ID
- 68788-7391_9522863c-9174-49fb-bf47-62b826b6b886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2016-09-27
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 125 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