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Aminocaproic Acid - 0409-4346-73 - (AMINOCAPROIC ACID)

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Drug Information of Aminocaproic Acid

Product NDC: 0409-4346
Proprietary Name: Aminocaproic Acid
Non Proprietary Name: AMINOCAPROIC ACID
Active Ingredient(s): 250    mg/mL & nbsp;   AMINOCAPROIC ACID
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aminocaproic Acid

Product NDC: 0409-4346
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070010
Marketing Category: ANDA
Start Marketing Date: 20110816

Package Information of Aminocaproic Acid

Package NDC: 0409-4346-73
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4346-73) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Aminocaproic Acid

NDC Code 0409-4346-73
Proprietary Name Aminocaproic Acid
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4346-73) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-4346
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMINOCAPROIC ACID
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110816
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name AMINOCAPROIC ACID
Strength Number 250
Strength Unit mg/mL
Pharmaceutical Classes Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]

Complete Information of Aminocaproic Acid


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