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    NDC 00069-1311-10 RETACRIT 20000 [iU]/mL Details

    RETACRIT 20000 [iU]/mL

    RETACRIT is a INTRAVENOUS; SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is EPOETIN.

    Product Information

    NDC 00069-1311
    Product ID 0069-1311_23aea279-5369-4735-9e43-7dfe3a38baf5
    Associated GPIs 82401020042050
    GCN Sequence Number 081714
    GCN Sequence Number Description epoetin alfa-epbx VIAL 20000/ML INJECTION
    HIC3 N1B
    HIC3 Description ERYTHROPOIESIS-STIMULATING AGENTS
    GCN 48911
    HICL Sequence Number 044931
    HICL Sequence Number Description EPOETIN ALFA-EPBX
    Brand/Generic Brand
    Proprietary Name RETACRIT
    Proprietary Name Suffix n/a
    Non-Proprietary Name epoetin alfa-epbx
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 20000
    Active Ingredient Units [iU]/mL
    Substance Name EPOETIN
    Labeler Name Pfizer Laboratories Div Pfizer Inc
    Pharmaceutical Class Erythropoiesis-stimulating Agent [EPC], Erythropoietin [CS], Increased Erythroid Cell Production [PE]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA125545
    Listing Certified Through 2024-12-31

    Package

    NDC 00069-1311-10 (00069131110)

    NDC Package Code 0069-1311-10
    Billing NDC 00069131110
    Package 10 VIAL, MULTI-DOSE in 1 CARTON (0069-1311-10) / 1 mL in 1 VIAL, MULTI-DOSE (0069-1311-01)
    Marketing Start Date 2020-11-09
    NDC Exclude Flag N
    Pricing Information N/A