NDC 60687-739 – Aminocaproic Acid

Aminocaproic Acid 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-739

Product details

Brand name
Aminocaproic Acid
Generic name
Aminocaproic Acid
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209060
Marketed since
March 10, 2023
Marketing end
April 30, 2028
Pharmacologic class
Antifibrinolytic Agent

Active ingredients

Uses, dosage, side effects and warnings for Aminocaproic Acid →

Package NDC codes (1)

Package NDCDescriptionSince
60687-739-2530 BLISTER PACK in 1 CARTON (60687-739-25) / 1 TABLET in 1 BLISTER PACK (60687-739-95)Mar 10, 2023

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