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Dipyridamole - 0555-0285-02 - (Dipyridamole)

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Drug Information of Dipyridamole

Product NDC: 0555-0285
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: 0555-0285
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087716
Marketing Category: ANDA
Start Marketing Date: 19820101

Package Information of Dipyridamole

Package NDC: 0555-0285-02
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0555-0285-02)

NDC Information of Dipyridamole

NDC Code 0555-0285-02
Proprietary Name Dipyridamole
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0555-0285-02)
Product NDC 0555-0285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dipyridamole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19820101
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name DIPYRIDAMOLE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of Dipyridamole


General Information