PERSANTINE Coated tablet Ref.[11063] Active ingredients: Dipyridamole

Source: FDA, National Drug Code (US)  Revision Year: 2019 

Product description

PERSANTINE (dipyridamole USP) is a platelet inhibitor chemically described as 2,2',2",2"'-[(4,8-Dipiperidinopyrimido[5,4-d]pyrimidine-2,6-diyl)dinitrilo]-tetraethanol.

It has the following structural formula:

Dipyridamole is an odorless yellow crystalline powder, having a bitter taste. It is soluble in dilute acids, methanol and chloroform, and practically insoluble in water.

PERSANTINE tablets for oral administration contain:

Active Ingredient:

TABLETS 25 mg, 50 mg, and 75 mg: dipyridamole USP 25 mg, 50 mg and 75 mg, respectively.

Inactive Ingredients:

TABLETS 25 mg, 50 mg, and 75 mg: acacia, carnauba wax, corn starch, edible white ink, lactose monohydrate, magnesium stearate, D&C yellow #10 aluminum lake, D&C red #30, helendon aluminum pink lake, sodium benzoate, methylparaben, propylparaben, polyethylene glycol, povidone, sucrose, talc, titanium dioxide, and white wax.

How Supplied

PERSANTINE tablets are available as round, orange, sugar-coated tablets of 25 mg, 50 mg and 75 mg coded BI/17, BI/18 and BI/19, respectively.

They are available in bottles of 100 tablets as indicated below:

  • 25 mg Tablets (NDC 0597-0017-01)
  • 50 mg Tablets (NDC 0597-0018-01)
  • 75 mg Tablets (NDC 0597-0019-01)

Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA

Product and trademark licensed from: Boehringer Ingelheim, International GmbH

Drugs

Drug Countries
PERSANTINE Canada, France, United States

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