Search by Drug Name or NDC

    NDC 53002-1202-03 Nortriptyline Hydrochloride 10 mg/1 Details

    Nortriptyline Hydrochloride 10 mg/1

    Nortriptyline Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is NORTRIPTYLINE HYDROCHLORIDE.

    Product Information

    NDC 53002-1202
    Product ID 53002-1202_64eee541-dbcb-448c-aafb-bc0dc7c3467f
    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 Nortriptyline Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Nortriptyline Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name NORTRIPTYLINE HYDROCHLORIDE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Tricyclic Antidepressant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074132
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1202-03 (53002120203)

    NDC Package Code 53002-1202-3
    Billing NDC 53002120203
    Package 30 CAPSULE in 1 BOTTLE (53002-1202-3)
    Marketing Start Date 2022-01-01
    NDC Exclude Flag N
    Pricing Information N/A