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    NDC 68788-7906-03 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 Preferred Pharmaceuticals Inc.. The primary component is PHENTERMINE HYDROCHLORIDE.

    Product Information

    NDC 68788-7906
    Product ID 68788-7906_a6e3706f-bcac-43d9-8cf9-567ab3884997
    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 Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA205008
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7906-03 (68788790603)

    NDC Package Code 68788-7906-3
    Billing NDC 68788790603
    Package 30 TABLET in 1 BOTTLE (68788-7906-3)
    Marketing Start Date 2021-05-18
    NDC Exclude Flag N
    Pricing Information N/A