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DIPYRIDAMOLE - 55154-4325-8 - (DIPYRIDAMOLE)

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Drug Information of DIPYRIDAMOLE

Product NDC: 55154-4325
Proprietary Name: DIPYRIDAMOLE
Non Proprietary Name: DIPYRIDAMOLE
Active Ingredient(s): 50    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: 55154-4325
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040782
Marketing Category: ANDA
Start Marketing Date: 20110805

Package Information of DIPYRIDAMOLE

Package NDC: 55154-4325-8
Package Description: 10 BLISTER PACK in 1 BAG (55154-4325-8) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of DIPYRIDAMOLE

NDC Code 55154-4325-8
Proprietary Name DIPYRIDAMOLE
Package Description 10 BLISTER PACK in 1 BAG (55154-4325-8) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-4325
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPYRIDAMOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110805
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name DIPYRIDAMOLE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of DIPYRIDAMOLE


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