ELIQUIS - 0003-0894-91 - (apixaban)

Alphabetical Index


Drug Information of ELIQUIS

Product NDC: 0003-0894
Proprietary Name: ELIQUIS
Non Proprietary Name: apixaban
Active Ingredient(s): 5    mg/1 & nbsp;   apixaban
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ELIQUIS

Product NDC: 0003-0894
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202155
Marketing Category: NDA
Start Marketing Date: 20121228

Package Information of ELIQUIS

Package NDC: 0003-0894-91
Package Description: 1 BLISTER PACK in 1 CARTON (0003-0894-91) > 14 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ELIQUIS

NDC Code 0003-0894-91
Proprietary Name ELIQUIS
Package Description 1 BLISTER PACK in 1 CARTON (0003-0894-91) > 14 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0003-0894
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name apixaban
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121228
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
Substance Name APIXABAN
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ELIQUIS


General Information