Search by Drug Name or NDC

    NDC 24658-0799-30 AMINOCAPROIC ACID 1000 mg/1 Details

    AMINOCAPROIC ACID 1000 mg/1

    AMINOCAPROIC ACID is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS. The primary component is AMINOCAPROIC ACID.

    Product Information

    NDC 24658-0799
    Product ID 24658-799_fc98e7a7-06f6-4036-b973-43fae1b77ccc
    Associated GPIs
    GCN Sequence Number 058109
    GCN Sequence Number Description aminocaproic acid TABLET 1000 MG ORAL
    HIC3 M9D
    HIC3 Description ANTIFIBRINOLYTIC AGENTS
    GCN 23444
    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 1000
    Active Ingredient Units mg/1
    Substance Name AMINOCAPROIC ACID
    Labeler Name PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
    Pharmaceutical Class Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213928
    Listing Certified Through 2024-12-31

    Package

    NDC 24658-0799-30 (24658079930)

    NDC Package Code 24658-799-30
    Billing NDC 24658079930
    Package 30 TABLET in 1 BOTTLE (24658-799-30)
    Marketing Start Date 2023-01-24
    NDC Exclude Flag N
    Pricing Information N/A