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DIPYRIDAMOLE - 42291-528-10 - (DIPYRIDAMOLE)

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Drug Information of DIPYRIDAMOLE

Product NDC: 42291-528
Proprietary Name: DIPYRIDAMOLE
Non Proprietary Name: DIPYRIDAMOLE
Active Ingredient(s): 75    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: 42291-528
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040782
Marketing Category: ANDA
Start Marketing Date: 20070708

Package Information of DIPYRIDAMOLE

Package NDC: 42291-528-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (42291-528-10)

NDC Information of DIPYRIDAMOLE

NDC Code 42291-528-10
Proprietary Name DIPYRIDAMOLE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (42291-528-10)
Product NDC 42291-528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPYRIDAMOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070708
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name DIPYRIDAMOLE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of DIPYRIDAMOLE


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