Skip to Content

Bisoprolol

Generic Name: Bisoprolol fumarate
Dosage Form: tablet, film coated

Medically reviewed by Drugs.com. Last updated on Jul 1, 2019.

Principal Display Panel

   

NDC 52817-270-30

Bisoprolol Fumarate Tablets, USP

5mg

Rx Only

30 Tablets

TruPharma

Principal Display Panel

NDC 52817-270-10

Bisoprolol Fumarate Tablets, USP

5mg

Rx Only

100 Tablets

TruPharma

Principal Display Panel

  

NDC 52817-271-30

Bisoprolol Fumarate Tablets, USP

10mg

Rx Only

30 Tablets

TruPharma

Principal Display Panel

  

NDC 52817-271-10

Bisoprolol Fumarate Tablets, USP

10mg

Rx Only

100 Tablets

TruPharma

Bisoprolol 
Bisoprolol fumarate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:52817-270
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Bisoprolol FUMARATE (Bisoprolol) Bisoprolol FUMARATE 5 mg
Inactive Ingredients
Ingredient Name Strength
CARNAUBA WAX  
SILICON DIOXIDE  
STARCH, CORN  
CROSPOVIDONE  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE  
HYPROMELLOSE, UNSPECIFIED  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POLYDEXTROSE  
POLYETHYLENE GLYCOL, UNSPECIFIED  
TITANIUM DIOXIDE  
TRIACETIN  
FD&C YELLOW NO. 6  
FD&C RED NO. 40  
FD&C BLUE NO. 2  
Product Characteristics
Color RED Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code MP;711
Contains     
Packaging
# Item Code Package Description
1 NDC:52817-270-10 100 TABLET, FILM COATED in 1 BOTTLE
2 NDC:52817-270-30 30 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075474 06/20/2019
Bisoprolol 
Bisoprolol fumarate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:52817-271
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Bisoprolol FUMARATE (Bisoprolol) Bisoprolol FUMARATE 10 mg
Inactive Ingredients
Ingredient Name Strength
CARNAUBA WAX  
SILICON DIOXIDE  
STARCH, CORN  
CROSPOVIDONE  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE  
HYPROMELLOSE, UNSPECIFIED  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POLYDEXTROSE  
POLYETHYLENE GLYCOL, UNSPECIFIED  
TITANIUM DIOXIDE  
TRIACETIN  
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 8mm
Flavor Imprint Code MP;712
Contains     
Packaging
# Item Code Package Description
1 NDC:52817-271-10 100 TABLET, FILM COATED in 1 BOTTLE
2 NDC:52817-271-30 30 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075474 06/20/2019
Labeler - TruPharma, LLC (078533947)
 
TruPharma, LLC
Hide