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Dipyridamole - 55390-555-10 - (Dipyridamole)

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Drug Information of Dipyridamole

Product NDC: 55390-555
Proprietary Name: Dipyridamole
Non Proprietary Name: Dipyridamole
Active Ingredient(s): 5    mg/mL & nbsp;   Dipyridamole
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dipyridamole

Product NDC: 55390-555
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074939
Marketing Category: ANDA
Start Marketing Date: 19980601

Package Information of Dipyridamole

Package NDC: 55390-555-10
Package Description: 10 VIAL in 1 BOX (55390-555-10) > 2 mL in 1 VIAL

NDC Information of Dipyridamole

NDC Code 55390-555-10
Proprietary Name Dipyridamole
Package Description 10 VIAL in 1 BOX (55390-555-10) > 2 mL in 1 VIAL
Product NDC 55390-555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dipyridamole
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19980601
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name DIPYRIDAMOLE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of Dipyridamole


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