Search by Drug Name or NDC

    NDC 75834-0291-05 Metoprolol Succinate 50 mg/1 Details

    Metoprolol Succinate 50 mg/1

    Metoprolol Succinate is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Nivagen Pharmaceuticals, Inc.. The primary component is METOPROLOL SUCCINATE.

    Product Information

    NDC 75834-0291
    Product ID 75834-291_0175a6b8-51dd-44d3-e063-6394a90a2f03
    Associated GPIs 33200030057520
    GCN Sequence Number 016599
    GCN Sequence Number Description metoprolol succinate TAB ER 24H 50 MG ORAL
    HIC3 J7C
    HIC3 Description BETA-ADRENERGIC BLOCKING AGENTS
    GCN 20741
    HICL Sequence Number 006323
    HICL Sequence Number Description METOPROLOL SUCCINATE
    Brand/Generic Generic
    Proprietary Name Metoprolol Succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metoprolol Succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name METOPROLOL SUCCINATE
    Labeler Name Nivagen Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203028
    Listing Certified Through 2024-12-31

    Package

    NDC 75834-0291-05 (75834029105)

    NDC Package Code 75834-291-05
    Billing NDC 75834029105
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-291-05)
    Marketing Start Date 2022-02-23
    NDC Exclude Flag N
    Pricing Information N/A