Search by Drug Name or NDC

    NDC 63304-0132-04 Doxycycline 100 mg/1 Details

    Doxycycline 100 mg/1

    Doxycycline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries Inc.. The primary component is DOXYCYCLINE.

    Product Information

    NDC 63304-0132
    Product ID 63304-132_fd417a50-69b5-40b4-89fd-58aea77ab547
    Associated GPIs 04000020000310
    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 Doxycycline
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxycycline
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE
    Labeler Name Sun Pharmaceutical Industries Inc.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065356
    Listing Certified Through 2024-12-31

    Package

    NDC 63304-0132-04 (63304013204)

    NDC Package Code 63304-132-04
    Billing NDC 63304013204
    Package 250 TABLET, FILM COATED in 1 BOTTLE (63304-132-04)
    Marketing Start Date 2018-08-06
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 8224b9c5-5c4b-4dda-bc58-47b6604c2884 Details

    Revised: 8/2018