Label: DIPYRIDAMOLE tablet, film coated

  • NDC Code(s): 64980-133-01, 64980-133-10, 64980-134-01, 64980-134-10, view more
    64980-135-01, 64980-135-10
  • Packager: Rising Pharmaceuticals, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 23, 2019

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Dipyridamole Tablets, USP

    25 mg, 50 mg, and 75 mg tablets

    Rx only

    Prescribing Information

  • DESCRIPTION

    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:

    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.

    Dipyridamole Tablets, USP 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: corn starch, hydroxypropyl methylcellulose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, and titanium dioxide.

  • CLINICAL PHARMACOLOGY

    It is believed that platelet reactivity and interaction with prosthetic cardiac valve surfaces, resulting in abnormally shortened platelet survival time, is a significant factor in thromboembolic complications occurring in connection with prosthetic heart valve replacement.

    Dipyridamole tablets have been found to lengthen abnormally shortened platelet survival time in a dose-dependent manner.

    In three randomized controlled clinical trials involving 854 patients who had undergone surgical placement of a prosthetic heart valve, dipyridamole tablets, in combination with warfarin, decreased the incidence of postoperative thromboembolic events by 62 to 91 % compared to warfarin treatment alone. The incidence of thromboembolic events in patients receiving the combination of dipyridamole tablets and warfarin ranged from 1.2 to 1.8%. In three additional studies involving 392 patients taking dipyridamole tablets and coumarin-like anticoagulants, the incidence of thromboembolic events ranged from 2.3 to 6.9%.

    In these trials, the coumarin anticoagulant was begun between 24 hours and 4 days postoperatively, and the dipyridamole tablets were begun between 24 hours and 10 days postoperatively. The length of follow-up in these trials varied from 1 to 2 years.

    Dipyridamole tablets do not influence prothrombin time or activity measurements when administered with warfarin.

    Mechanism of Action

    Dipyridamole inhibits the uptake of adenosine into platelets, endothelial cells and erythrocytes in vitro and in vivo; the inhibition occurs in a dose-dependent manner at therapeutic concentrations (0.5-1.9 μg/mL). This inhibition results in an increase in local concentrations of adenosine which acts on the platelet A 2-receptor thereby stimulating platelet adenylate cyclase and increasing platelet cyclic-3',5'- adenosine monophosphate (cAMP) levels. Via this mechanism, platelet aggregation is inhibited in response to various stimuli such as platelet activating factor (PAF), collagen and adenosine diphosphate (ADP).

    Dipyridamole inhibits phosphodiesterase (PDE) in various tissues. While the inhibition of cAMP-PDE is weak, therapeutic levels of dipyridamole inhibit cyclic-3',5'-guanosine monophosphate-PDE (cGMP- PDE), thereby augmenting the increase in cGMP produced by EDRF (endothelium-derived relaxing factor, now identified as nitric oxide).

    Hemodynamics

    In dogs intraduodenal doses of dipyridamole of 0.5 to 4.0 mg/kg produced dose-related decreases in systemic and coronary vascular resistance leading to decreases in systemic blood pressure and increases in coronary blood flow. Onset of action was in about 24 minutes and effects persisted for about 3 hours.

    Similar effects were observed following intravenous dipyridamole in doses ranging from 0.025 to 2.0 mg/kg.

    In man the same qualitative hemodynamic effects have been observed. However, acute intravenous administration of dipyridamole may worsen regional myocardial perfusion distal to partial occlusion of coronary arteries.

    Pharmacokinetics and Metabolism

    Following an oral dose of dipyridamole tablets, the average time to peak concentration is about 75 minutes. The decline in plasma concentration following a dose of dipyridamole tablets fits a two-compartment model. The alpha half-life (the initial decline following peak concentration) is approximately 40 minutes. The beta half-life (the terminal decline in plasma concentration) is approximately 10 hours. Dipyridamole is highly bound to plasma proteins. It is metabolized in the liver where it is conjugated as a glucuronide and excreted with the bile.

  • INDICATIONS AND USAGE

    Dipyridamole tablets are indicated as an adjunct to coumarin anticoagulants in the prevention of postoperative thromboembolic complications of cardiac valve replacement.

  • CONTRAINDICATIONS

    Hypersensitivity to dipyridamole and any of the other components.

  • PRECAUTIONS

    General

    Coronary Artery Disease: Dipyridamole has a vasodilatory effect and should be used with caution in patients with severe coronary artery disease (e.g., unstable angina or recently sustained myocardial infarction). Chest pain may be aggravated in patients with underlying coronary artery disease who are receiving dipyridamole.

    Hepatic Insufficiency: Elevations of hepatic enzymes and hepatic failure have been reported in association with dipyridamole administration.

    Hypotension: Dipyridamole should be used with caution in patients with hypotension since it can produce peripheral vasodilation.

    Stress Testing with Intravenous Dipyridamole and Other Adenosinergic Agents: Clinical experience suggests that patients being treated with dipyridamole tablets who also require pharmacological stress testing with intravenous dipyridamole or other adenosinergic agents (e.g. adenosine, regadenoson) should interrupt dipyridamole tablets for 48 hours prior to stress testing.

    Intake of dipyridamole tablets within 48 hours prior to stress testing with intravenous dipyridamole or other adenosinergic agents may increase the risk for cardiovascular side effects of these agents and may impair the sensitivity of the test.

    Laboratory Tests

    Dipyridamole has been associated with elevated hepatic enzymes.

    Drug Interactions

    No pharmacokinetic drug-drug interaction studies were conducted with dipyridamole tablets. The following information was obtained from the literature.

    Adenosinergic agents (e.g., adenosine, regadenoson): Dipyridamole has been reported to increase the plasma levels and cardiovascular effects of adenosine. Adjustment of adenosine dosage may be necessary. Dipyridamole also increases the cardiovascular effects of regadenoson, an adenosine A 2A-receptor agonist. The potential risk of cardiovascular side effects with intravenous adenosinergic agents may be increased during the testing period when dipyridamole is not held 48 hours prior to stress testing.

    Cholinesterase Inhibitors: Dipyridamole may counteract the anticholinesterase effect of cholinesterase inhibitors, thereby potentially aggravating myasthenia gravis.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    In studies in which dipyridamole was administered in the feed to mice (up to 111 weeks in males and females) and rats (up to 128 weeks in males and up to 142 weeks in females), there was no evidence of drug-related carcinogenesis. The highest dose administered in these studies (75 mg/kg/day) was, on a mg/m 2 basis, about equivalent to the maximum recommended daily human oral dose (MRHD) in mice and about twice the MRHD in rats. Mutagenicity tests of dipyridamole with bacterial and mammalian cell systems were negative. There was no evidence of impaired fertility when dipyridamole was administered to male and female rats at oral doses up to 500 mg/kg/day (about 12 times the MRHD on a mg/m 2 basis). A significant reduction in number of corpora lutea with consequent reduction in implantations and live fetuses was, however, observed at 1250 mg/kg (more than 30 times the MRHD on a mg/m 2 basis).

    Pregnancy

    Teratogenic Effects

    Reproduction studies have been performed in mice, rabbits and rats at oral dipyridamole doses of up to 125 mg/kg, 40 mg/kg and 1000 mg/kg, respectively (about 1 ½, 2 and 25 times the maximum recommended daily human oral dose, respectively, on a mg/m 2 basis) and have revealed no evidence of harm to the fetus due to dipyridamole. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, dipyridamole tablets should be used during pregnancy only if clearly needed.

    Nursing Mothers

    As dipyridamole is excreted in human milk, caution should be exercised when dipyridamole tablets are administered to a nursing woman.

    Pediatric Use

    Safety and effectiveness in the pediatric population below the age of 12 years have not been established.

  • ADVERSE REACTIONS

    Adverse reactions at therapeutic doses are usually minimal and transient. On long-term use of dipyridamole tablets initial side effects usually disappear. The following reactions in Table 1 were reported in two heart valve replacement trials comparing dipyridamole tablets and warfarin therapy to either warfarin alone or warfarin and  placebo:

    Table 1 Adverse Reactions Reported in 2 Heart Valve Replacement Trials
    Adverse
    Reaction
    Dipyridamole Tablets/
    Warfarin
    Placebo/
    Warfarin
    Number of patients 147 170
    Dizziness 13.6% 8.2%
    Abdominal distress 6.1% 3.5%
    Headache 2.3% 0.0%
    Rash 2.3% 1.1%

    Other reactions from uncontrolled studies include diarrhea, vomiting, flushing and pruritus. In addition, angina pectoris has been reported rarely and there have been rare reports of liver dysfunction. On those uncommon occasions when adverse reactions have been persistent or intolerable, they have ceased on withdrawal of the medication.

    When dipyridamole tablets were administered concomitantly with warfarin, bleeding was no greater in frequency or severity than that observed when warfarin was administered alone. In rare cases, increased bleeding during or after surgery has been observed.

    In post-marketing reporting experience, there have been rare reports of hypersensitivity reactions (such as rash, urticaria, severe bronchospasm, and angioedema), larynx edema, fatigue, malaise, myalgia, arthritis, nausea, dyspepsia, paresthesia, hepatitis, thrombocytopenia, alopecia, cholelithiasis, hypotension, palpitation, and tachycardia.

  • OVERDOSAGE

    In case of real or suspected overdose, seek medical attention or contact a Poison Control Center immediately. Careful medical management is essential. Based upon the known hemodynamic effects of dipyridamole, symptoms such as warm feeling, flushes, sweating, restlessness, feeling of weakness and dizziness may occur. A drop in blood pressure and tachycardia might also be observed.

    Symptomatic treatment is recommended, possibly including a vasopressor drug. Gastric lavage should be considered. Administration of xanthine derivatives (e.g., aminophylline) may reverse the hemodynamic effects of dipyridamole overdose. Since dipyridamole is highly protein bound, dialysis is not likely to be of benefit.

  • DOSAGE AND ADMINISTRATION

    Adjunctive Use in Prophylaxis of Thromboembolism after Cardiac Valve Replacement. The recommended dose is 75 mg to 100 mg four times daily as an adjunct to the usual warfarin therapy. Please note that aspirin is not to be administered concomitantly with coumarin anticoagulants.

  • HOW SUPPLIED

    Dipyridamole Tablets, USP are available as round, white, film-coated tablets of 25 mg, 50 mg, and 75 mg coded 81/SL, 82/SL, and 83/SL, respectively.

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

    25 mg Tablets (NDC 64980-133-01)

    50 mg Tablets (NDC 64980-134-01)

    75 mg Tablets (NDC 64980-135-01)

    They are available in bottles of 1000 tablets as indicated below:

    25 mg Tablets (NDC 64980-133-10)

    50 mg Tablets (NDC 64980-134-10)

    75 mg Tablets (NDC 64980-135-10)

    Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F) [see USP Controlled Room Temperature]. Keep out of reach of children.

    For medical inquiries, please visit the website www.risingpharma.com or call 1-866-562-4597.

    Distributed by:
    Rising Pharmaceuticals, Inc.,  
    Saddle Brook, NJ 07663 USA

    Manufactured by:
    Murty Pharmaceuticals, Inc., 
    Lexington, KY 40509 USA

    Revised: December 2019 

    P112-03

  • PRINCIPAL DISPLAY PANEL

    Container 25 mg

    Rising            NDC 64980-133-01

    Dipyridamole
    Tablets, USP

    25 mg

    100 Tablets

    Rx only

    Rising            NDC 64980-133-01
Dipyridamole
Tablets, USP
25 mg
100 Tablets

Rx only

  • PRINCIPAL DISPLAY PANEL

    Container 25 mg

    Rising            NDC 64980-133-10

    Dipyridamole
    Tablets, USP

    25 mg

    1000 Tablets

    Rx only

    Container 25 mg
Rising            NDC 64980-133-10
Dipyridamole
Tablets, USP
25 mg
1000 Tablets

Rx only

  • PRINCIPAL DISPLAY PANEL

    Container 50 mg

    Rising            NDC 64980-134-01

    Dipyridamole
    Tablets, USP

    50 mg

    100 Tablets

    Rx only

    Rising            NDC 64980-134-01
Dipyridamole
Tablets, USP
50 mg
100 Tablets

Rx only

  • PRINCIPAL DISPLAY PANEL

    Container 50 mg

    Rising            NDC 64980-134-10

    Dipyridamole
    Tablets, USP

    50 mg

    1000 Tablets

    Rx only

    Container 50 mg
Rising            NDC 64980-134-10
Dipyridamole
Tablets, USP
50 mg
1000 Tablets

Rx only

  • PRINCIPAL DISPLAY PANEL

    Container 75 mg

    Rising            NDC 64980-135-01

    Dipyridamole
    Tablets, USP

    75 mg

    100 Tablets

    Rx only

    Rising            NDC 64980-135-01
Dipyridamole
Tablets, USP
75 mg
100 Tablets

Rx only

  • PRINCIPAL DISPLAY PANEL

    Container 75 mg

    Rising            NDC 64980-135-10

    Dipyridamole
    Tablets, USP

    75 mg

    1000 Tablets

    Rx only

    Container 75 mg
Rising            NDC 64980-135-10
Dipyridamole
Tablets, USP
75 mg
1000 Tablets

Rx only

  • INGREDIENTS AND APPEARANCE
    DIPYRIDAMOLE 
    dipyridamole tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64980-133
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPYRIDAMOLE (UNII: 64ALC7F90C) (DIPYRIDAMOLE - UNII:64ALC7F90C) DIPYRIDAMOLE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code SL;81
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64980-133-01100 in 1 BOTTLE; Type 0: Not a Combination Product08/05/2007
    2NDC:64980-133-101000 in 1 BOTTLE; Type 0: Not a Combination Product08/05/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA04073308/05/2007
    DIPYRIDAMOLE 
    dipyridamole tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64980-134
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPYRIDAMOLE (UNII: 64ALC7F90C) (DIPYRIDAMOLE - UNII:64ALC7F90C) DIPYRIDAMOLE50 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize8mm
    FlavorImprint Code SL;82
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64980-134-01100 in 1 BOTTLE; Type 0: Not a Combination Product02/13/2007
    2NDC:64980-134-101000 in 1 BOTTLE; Type 0: Not a Combination Product02/13/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA04073302/13/2007
    DIPYRIDAMOLE 
    dipyridamole tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:64980-135
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPYRIDAMOLE (UNII: 64ALC7F90C) (DIPYRIDAMOLE - UNII:64ALC7F90C) DIPYRIDAMOLE75 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE (UNII: FZ989GH94E)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code SL;83
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64980-135-01100 in 1 BOTTLE; Type 0: Not a Combination Product02/13/2007
    2NDC:64980-135-101000 in 1 BOTTLE; Type 0: Not a Combination Product02/13/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA04073302/13/2007
    Labeler - Rising Pharmaceuticals, Inc. (041241766)
    Registrant - Murty Pharmaceuticals, Inc. (943117366)