Search by Drug Name or NDC

    NDC 68462-0356-05 Theophylline 600 mg/1 Details

    Theophylline 600 mg/1

    Theophylline is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., USA. The primary component is THEOPHYLLINE ANHYDROUS.

    Product Information

    NDC 68462-0356
    Product ID 68462-356_aaa6684e-4eef-42a8-92b6-8f317e570903
    Associated GPIs 44300040007560
    GCN Sequence Number 011810
    GCN Sequence Number Description theophylline anhydrous TAB ER 24H 600 MG ORAL
    HIC3 A1B
    HIC3 Description XANTHINES
    GCN 00417
    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 TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name THEOPHYLLINE ANHYDROUS
    Labeler Name Glenmark Pharmaceuticals Inc., USA
    Pharmaceutical Class Methylxanthine [EPC], Xanthines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090355
    Listing Certified Through 2025-12-31

    Package

    NDC 68462-0356-05 (68462035605)

    NDC Package Code 68462-356-05
    Billing NDC 68462035605
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-05)
    Marketing Start Date 2010-07-13
    NDC Exclude Flag N
    Pricing Information N/A