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Aminocaproic Acid - 61748-045-01 - (Aminocaproic Acid)

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Drug Information of Aminocaproic Acid

Product NDC: 61748-045
Proprietary Name: Aminocaproic Acid
Non Proprietary Name: Aminocaproic Acid
Active Ingredient(s): 500    mg/1 & nbsp;   Aminocaproic Acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Aminocaproic Acid

Product NDC: 61748-045
Labeler Name: VersaPharm Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075602
Marketing Category: ANDA
Start Marketing Date: 20010801

Package Information of Aminocaproic Acid

Package NDC: 61748-045-01
Package Description: 100 TABLET in 1 BOTTLE (61748-045-01)

NDC Information of Aminocaproic Acid

NDC Code 61748-045-01
Proprietary Name Aminocaproic Acid
Package Description 100 TABLET in 1 BOTTLE (61748-045-01)
Product NDC 61748-045
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aminocaproic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010801
Marketing Category Name ANDA
Labeler Name VersaPharm Incorporated
Substance Name AMINOCAPROIC ACID
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]

Complete Information of Aminocaproic Acid


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