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    NDC 50436-0250-01 Phentermine Hydrochloride 37.5 mg/1 Details

    Phentermine Hydrochloride 37.5 mg/1

    Phentermine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Unit Dose Services. The primary component is PHENTERMINE HYDROCHLORIDE.

    Product Information

    NDC 50436-0250
    Product ID 50436-0250_dbfd6ac5-be2c-4a60-96da-4fa5bbd15f88
    Associated GPIs 61200070100310
    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 Phentermine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Phentermine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 37.5
    Active Ingredient Units mg/1
    Substance Name PHENTERMINE HYDROCHLORIDE
    Labeler Name Unit Dose Services
    Pharmaceutical Class Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA040876
    Listing Certified Through 2024-12-31

    Package

    NDC 50436-0250-01 (50436025001)

    NDC Package Code 50436-0250-1
    Billing NDC 50436025001
    Package 7 TABLET in 1 BOTTLE (50436-0250-1)
    Marketing Start Date 2017-07-07
    NDC Exclude Flag N
    Pricing Information N/A