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    NDC 42689-0013-01 Propranolol Hydrochloride 120 mg/1 Details

    Propranolol Hydrochloride 120 mg/1

    Propranolol Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Nortec Development Associates, Inc. The primary component is PROPRANOLOL HYDROCHLORIDE.

    Product Information

    NDC 42689-0013
    Product ID 42689-013_0a5bc268-a231-1779-e063-6294a90aa769
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Propranolol Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Propranolol Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 120
    Active Ingredient Units mg/1
    Substance Name PROPRANOLOL HYDROCHLORIDE
    Labeler Name Nortec Development Associates, Inc
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078065
    Listing Certified Through 2024-12-31

    Package

    NDC 42689-0013-01 (42689001301)

    NDC Package Code 42689-013-01
    Billing NDC 42689001301
    Package 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42689-013-01)
    Marketing Start Date 2015-05-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 42689-0012-10 42689-0013-10 >>

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