Cephalexin

Product NDC
51655-125
11-digit product format
516550125
Labeler code
51655
Product ID
51655-125_4afc9b83-70f5-4d70-a7e2-6fb333dd7ae6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
CAPSULE
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA065229
Marketing category
ANDA
Marketing start
2014-06-20
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#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEPHALEXINACTIVE INGREDIENTOBN7UDS42YCEPHALEXIN CAPSULE [NORTHWIND PHARMACEUTICALS]3
CEPHALEXIN ANHYDROUSACTIVE MOIETY5SFF1W6677CEPHALEXIN CAPSULE [NORTHWIND PHARMACEUTICALS]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-125CEPHALEXIN CAPSULE [NORTHWIND PHARMACEUTICALS]3Legacy NDC20141001_694e406b-0dbd-47ef-b176-64d78ca836fa.zip