BARACLUDE - 0003-1614-12 - (entecavir)

Alphabetical Index


Drug Information of BARACLUDE

Product NDC: 0003-1614
Proprietary Name: BARACLUDE
Non Proprietary Name: entecavir
Active Ingredient(s): .05    mg/mL & nbsp;   entecavir
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BARACLUDE

Product NDC: 0003-1614
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021798
Marketing Category: NDA
Start Marketing Date: 20050329

Package Information of BARACLUDE

Package NDC: 0003-1614-12
Package Description: 1 BOTTLE in 1 CARTON (0003-1614-12) > 210 mL in 1 BOTTLE

NDC Information of BARACLUDE

NDC Code 0003-1614-12
Proprietary Name BARACLUDE
Package Description 1 BOTTLE in 1 CARTON (0003-1614-12) > 210 mL in 1 BOTTLE
Product NDC 0003-1614
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name entecavir
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20050329
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
Substance Name ENTECAVIR
Strength Number .05
Strength Unit mg/mL
Pharmaceutical Classes Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of BARACLUDE


General Information