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    NDC 42291-0525-10 propranolol hydrochloride 160 mg/1 Details

    propranolol hydrochloride 160 mg/1

    propranolol hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is PROPRANOLOL HYDROCHLORIDE.

    Product Information

    NDC 42291-0525
    Product ID 42291-525_0e902405-2b12-fc76-e063-6394a90ad984
    Associated GPIs 33100040107040
    GCN Sequence Number 005114
    GCN Sequence Number Description propranolol HCl CAP SA 24H 160 MG ORAL
    HIC3 J7C
    HIC3 Description BETA-ADRENERGIC BLOCKING AGENTS
    GCN 03232
    HICL Sequence Number 002101
    HICL Sequence Number Description PROPRANOLOL HCL
    Brand/Generic Generic
    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 160
    Active Ingredient Units mg/1
    Substance Name PROPRANOLOL HYDROCHLORIDE
    Labeler Name AvKARE
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078703
    Listing Certified Through 2025-12-31

    Package

    NDC 42291-0525-10 (42291052510)

    NDC Package Code 42291-525-10
    Billing NDC 42291052510
    Package 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-525-10)
    Marketing Start Date 2017-07-31
    NDC Exclude Flag N
    Pricing Information N/A