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    NDC 71205-0898-30 Albuterol 2 mg/1 Details

    Albuterol 2 mg/1

    Albuterol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is ALBUTEROL SULFATE.

    Product Information

    NDC 71205-0898
    Product ID 71205-898_f5ac6375-7f17-4d27-b13a-b44e73281838
    Associated GPIs 44201010100305
    GCN Sequence Number 005033
    GCN Sequence Number Description albuterol sulfate TABLET 2 MG ORAL
    HIC3 J5D
    HIC3 Description BETA-ADRENERGIC AGENTS
    GCN 20100
    HICL Sequence Number 002073
    HICL Sequence Number Description ALBUTEROL SULFATE
    Brand/Generic Generic
    Proprietary Name Albuterol
    Proprietary Name Suffix n/a
    Non-Proprietary Name albuterol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2
    Active Ingredient Units mg/1
    Substance Name ALBUTEROL SULFATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207046
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0898-30 (71205089830)

    NDC Package Code 71205-898-30
    Billing NDC 71205089830
    Package 30 TABLET in 1 BOTTLE (71205-898-30)
    Marketing Start Date 2021-07-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 895dff1c-d21c-4470-b021-a5b68364c1ec Details

    Revised: 4/2022