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    NDC 47335-0037-40 HYDROXYPROGESTERONE CAPROATE 250 mg/mL Details

    HYDROXYPROGESTERONE CAPROATE 250 mg/mL

    HYDROXYPROGESTERONE CAPROATE is a INTRAMUSCULAR INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is HYDROXYPROGESTERONE CAPROATE.

    Product Information

    NDC 47335-0037
    Product ID 47335-037_dd6cda1c-d74f-4cc0-8027-bc2af7c1b1f6
    Associated GPIs
    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 HYDROXYPROGESTERONE CAPROATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name HYDROXYPROGESTERONE CAPROATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAMUSCULAR
    Active Ingredient Strength 250
    Active Ingredient Units mg/mL
    Substance Name HYDROXYPROGESTERONE CAPROATE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Progesterone Congeners [CS], Progestin [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208381
    Listing Certified Through 2024-12-31

    Package

    NDC 47335-0037-40 (47335003740)

    NDC Package Code 47335-037-40
    Billing NDC 47335003740
    Package 1 VIAL, MULTI-DOSE in 1 CARTON (47335-037-40) / 5 mL in 1 VIAL, MULTI-DOSE
    Marketing Start Date 2019-07-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 458ed273-ef9c-4351-8bc2-173c3059d107 Details

    Revised: 4/2019