Search by Drug Name or NDC

    NDC 69238-1637-03 Aminocaproic acid 500 mg/1 Details

    Aminocaproic acid 500 mg/1

    Aminocaproic acid is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is AMINOCAPROIC ACID.

    Product Information

    NDC 69238-1637
    Product ID 69238-1637_6091bbf2-e45e-416d-bd4e-fc95dfeb609a
    Associated GPIs 84100010000305
    GCN Sequence Number 006504
    GCN Sequence Number Description aminocaproic acid TABLET 500 MG ORAL
    HIC3 M9D
    HIC3 Description ANTIFIBRINOLYTIC AGENTS
    GCN 25590
    HICL Sequence Number 002801
    HICL Sequence Number Description AMINOCAPROIC ACID
    Brand/Generic Generic
    Proprietary Name Aminocaproic acid
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aminocaproic acid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name AMINOCAPROIC ACID
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212492
    Listing Certified Through 2024-12-31

    Package

    NDC 69238-1637-03 (69238163703)

    NDC Package Code 69238-1637-3
    Billing NDC 69238163703
    Package 30 TABLET in 1 BOTTLE, PLASTIC (69238-1637-3)
    Marketing Start Date 2019-11-30
    NDC Exclude Flag N
    Pricing Information N/A