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    NDC 00115-1685-01 Dexmethylphenidate hydrochloride 20 mg/1 Details

    Dexmethylphenidate hydrochloride 20 mg/1

    Dexmethylphenidate hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is DEXMETHYLPHENIDATE HYDROCHLORIDE.

    Product Information

    NDC 00115-1685
    Product ID 0115-1685_d431fe33-4a29-4d90-9d0d-38f146aedbd6
    Associated GPIs 61400016107040
    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 Dexmethylphenidate hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dexmethylphenidate hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name DEXMETHYLPHENIDATE HYDROCHLORIDE
    Labeler Name Amneal Pharmaceuticals of New York LLC
    Pharmaceutical Class Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA079108
    Listing Certified Through 2024-12-31

    Package

    NDC 00115-1685-01 (00115168501)

    NDC Package Code 0115-1685-01
    Billing NDC 00115168501
    Package 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1685-01)
    Marketing Start Date 2015-12-21
    NDC Exclude Flag N
    Pricing Information N/A
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