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    NDC 00121-4820-40 THEOPHYLLINE 80 mg/15mL Details

    THEOPHYLLINE 80 mg/15mL

    THEOPHYLLINE is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PAI Holdings, LLC. The primary component is THEOPHYLLINE.

    Product Information

    NDC 00121-4820
    Product ID 0121-4820_30282017-c9a7-4a0d-8c87-468e2feba567
    Associated GPIs 44300040002010
    GCN Sequence Number 070185
    GCN Sequence Number Description theophylline anhydrous ELIXIR 80 MG/15ML ORAL
    HIC3 A1B
    HIC3 Description XANTHINES
    GCN 33547
    HICL Sequence Number 000025
    HICL Sequence Number Description THEOPHYLLINE ANHYDROUS
    Brand/Generic Generic
    Proprietary Name THEOPHYLLINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name THEOPHYLLINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/15mL
    Substance Name THEOPHYLLINE
    Labeler Name PAI Holdings, LLC
    Pharmaceutical Class Methylxanthine [EPC], Xanthines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206344
    Listing Certified Through 2024-12-31

    Package

    NDC 00121-4820-40 (00121482040)

    NDC Package Code 0121-4820-40
    Billing NDC 00121482040
    Package 4 TRAY in 1 CASE (0121-4820-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4820-15)
    Marketing Start Date 2016-12-16
    NDC Exclude Flag N
    Pricing Information N/A