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    NDC 70121-1609-05 Methylprednisolone acetate 40 mg/mL Details

    Methylprednisolone acetate 40 mg/mL

    Methylprednisolone acetate is a INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE INJECTION, SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is METHYLPREDNISOLONE ACETATE.

    Product Information

    NDC 70121-1609
    Product ID 70121-1609_1f4ff988-a647-4ed8-bc8b-cfa13b037cee
    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 Methylprednisolone acetate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methylprednisolone acetate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SUSPENSION
    Route INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
    Active Ingredient Strength 40
    Active Ingredient Units mg/mL
    Substance Name METHYLPREDNISOLONE ACETATE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA216502
    Listing Certified Through 2024-12-31

    Package

    NDC 70121-1609-05 (70121160905)

    NDC Package Code 70121-1609-5
    Billing NDC 70121160905
    Package 25 VIAL, MULTI-DOSE in 1 CARTON (70121-1609-5) / 10 mL in 1 VIAL, MULTI-DOSE
    Marketing Start Date 2023-11-10
    NDC Exclude Flag N
    Pricing Information N/A