FDA.reportPublic FDA data

Cephalexin

Product NDC
51655-026
11-digit product format
516550026
Labeler code
51655
Product ID
51655-026_18dbd24a-dd4b-4e2a-be9c-02d48078122c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA065253
Marketing category
ANDA
Marketing start
2014-07-18
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-026-522026-01-06C16284748780-19d75b9d0-3955-f424-e053-dadaa90a57ce41c59e38-37bd-4f3a-8b06-6be03012f537
51655-026-842026-01-06C16284748780-19d75b9d0-3955-f424-e053-dadaa90a57ce41c59e38-37bd-4f3a-8b06-6be03012f537
51655-026-522020-01-31C16284748780-19d75b9d0-3955-f424-e053-dadaa90a57ce41c59e38-37bd-4f3a-8b06-6be03012f537
51655-026-842020-01-31C16284748780-19d75b9d0-3955-f424-e053-dadaa90a57ce41c59e38-37bd-4f3a-8b06-6be03012f537

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CEPHALEXINACTIVE INGREDIENTOBN7UDS42YCEPHALEXIN TABLET [NORTHWIND PHARMACEUTICALS, LLC]2
CEPHALEXIN ANHYDROUSACTIVE MOIETY5SFF1W6677CEPHALEXIN TABLET [NORTHWIND PHARMACEUTICALS, LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-026CEPHALEXIN TABLET [NORTHWIND PHARMACEUTICALS, LLC]2Legacy NDC20141110_41c59e38-37bd-4f3a-8b06-6be03012f537.zip