Strength
1000 mg/1
Manufacturer
Hikma Pharmaceuticals USA Inc.NDC
00054111013
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
6/18/2025
Active Ingredients
AMINOCAPROIC ACIDApproval Type
Authorized Generic (NDA)
FDA Application
NDA015197On Market Since
3/12/2019
Pharmacological Classes
Antifibrinolytic Agent
Decreased Fibrinolysis
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