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DIPYRIDAMOLE - 64980-135-10 - (DIPYRIDAMOLE)

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Drug Information of DIPYRIDAMOLE

Product NDC: 64980-135
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: 64980-135
Labeler Name: Rising Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040733
Marketing Category: ANDA
Start Marketing Date: 20070213

Package Information of DIPYRIDAMOLE

Package NDC: 64980-135-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (64980-135-10)

NDC Information of DIPYRIDAMOLE

NDC Code 64980-135-10
Proprietary Name DIPYRIDAMOLE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (64980-135-10)
Product NDC 64980-135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPYRIDAMOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070213
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals, 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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