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    NDC 70594-0085-02 Ampicillin 500 mg/1 Details

    Ampicillin 500 mg/1

    Ampicillin is a INTRAVENOUS INJECTION, POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Xellia Pharmaceuticals USA LLC. The primary component is AMPICILLIN SODIUM.

    Product Information

    NDC 70594-0085
    Product ID 70594-085_2c29bd08-f467-4028-aac6-0a5b3007a5d3
    Associated GPIs 01200020302115
    GCN Sequence Number 008937
    GCN Sequence Number Description ampicillin sodium VIAL 500 MG INJECTION
    HIC3 W1A
    HIC3 Description PENICILLIN ANTIBIOTICS
    GCN 39245
    HICL Sequence Number 003952
    HICL Sequence Number Description AMPICILLIN SODIUM
    Brand/Generic Generic
    Proprietary Name Ampicillin
    Proprietary Name Suffix n/a
    Non-Proprietary Name AMPICILLIN SODIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, POWDER, FOR SOLUTION
    Route INTRAVENOUS
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name AMPICILLIN SODIUM
    Labeler Name Xellia Pharmaceuticals USA LLC
    Pharmaceutical Class Penicillin-class Antibacterial [EPC], Penicillins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090583
    Listing Certified Through 2024-12-31

    Package

    NDC 70594-0085-02 (70594008502)

    NDC Package Code 70594-085-02
    Billing NDC 70594008502
    Package 10 VIAL in 1 CARTON (70594-085-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-085-01)
    Marketing Start Date 2021-01-10
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 94421dac-7865-49f8-ae52-871eee6465ac Details

    Revised: 10/2021