Cephalexin
- Product NDC
- 51655-720
- 11-digit product format
- 516550720
- Labeler code
- 51655
- Product ID
- 51655-720_7307d314-f1cd-74f1-e053-2a91aa0a01b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA065248
- Marketing category
- ANDA
- Marketing start
- 2015-10-09
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#