AMICAR - 49411-051-01 - (Aminocaproic Acid)

Alphabetical Index


Drug Information of AMICAR

Product NDC: 49411-051
Proprietary Name: AMICAR
Non Proprietary Name: Aminocaproic Acid
Active Ingredient(s): 1000    mg/1 & nbsp;   Aminocaproic Acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AMICAR

Product NDC: 49411-051
Labeler Name: Clover Pharmaceuticals Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA015197
Marketing Category: NDA
Start Marketing Date: 20120411

Package Information of AMICAR

Package NDC: 49411-051-01
Package Description: 100 TABLET in 1 BOTTLE (49411-051-01)

NDC Information of AMICAR

NDC Code 49411-051-01
Proprietary Name AMICAR
Package Description 100 TABLET in 1 BOTTLE (49411-051-01)
Product NDC 49411-051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aminocaproic Acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120411
Marketing Category Name NDA
Labeler Name Clover Pharmaceuticals Corp.
Substance Name AMINOCAPROIC ACID
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]

Complete Information of AMICAR


General Information