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Dipyridamole - 54868-0042-1 - (dipyridamole)

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Drug Information of Dipyridamole

Product NDC: 54868-0042
Proprietary Name: Dipyridamole
Non Proprietary Name: dipyridamole
Active Ingredient(s): 25    mg/1 & nbsp;   dipyridamole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Dipyridamole

Product NDC: 54868-0042
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088999
Marketing Category: ANDA
Start Marketing Date: 20090807

Package Information of Dipyridamole

Package NDC: 54868-0042-1
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (54868-0042-1)

NDC Information of Dipyridamole

NDC Code 54868-0042-1
Proprietary Name Dipyridamole
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (54868-0042-1)
Product NDC 54868-0042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dipyridamole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090807
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DIPYRIDAMOLE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of Dipyridamole


General Information