NDC 0009-0280

Depo-Medrol

Methylprednisolone Acetate

Depo-Medrol is a Intralesional; Intramuscular; Intrasynovial; Soft Tissue Injection, Suspension in the Human Prescription Drug category. It is labeled and distributed by Pharmacia & Upjohn Company Llc. The primary component is Methylprednisolone Acetate.

Product ID0009-0280_0feb225a-2e17-4681-8f7a-fa7c114a7c11
NDC0009-0280
Product TypeHuman Prescription Drug
Proprietary NameDepo-Medrol
Generic NameMethylprednisolone Acetate
Dosage FormInjection, Suspension
Route of AdministrationINTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Marketing Start Date1959-05-28
Marketing CategoryNDA / NDA
Application NumberNDA011757
Labeler NamePharmacia & Upjohn Company LLC
Substance NameMETHYLPREDNISOLONE ACETATE
Active Ingredient Strength40 mg/mL
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0009-0280-02

1 VIAL, MULTI-DOSE in 1 CARTON (0009-0280-02) > 5 mL in 1 VIAL, MULTI-DOSE
Marketing Start Date1959-05-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0009-0280-25 [00009028025]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-30
Marketing End Date2014-03-30

NDC 0009-0280-03 [00009028003]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1959-05-28

NDC 0009-0280-51 [00009028051]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1959-05-28

NDC 0009-0280-02 [00009028002]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1959-05-28

NDC 0009-0280-52 [00009028052]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1959-05-28

NDC 0009-0280-24 [00009028024]

Depo-Medrol INJECTION, SUSPENSION
Marketing CategoryNDA
Application NumberNDA011757
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-30
Marketing End Date2014-03-30

Drug Details

Active Ingredients

IngredientStrength
METHYLPREDNISOLONE ACETATE40 mg/mL

OpenFDA Data

SPL SET ID:823b0010-2b57-4e76-b5ac-4a8c2963438f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1358510
  • 1358512
  • 1358619
  • 1358617
  • 1358612
  • 1358610
    • UPC Code
  • 0300090306021
  • 0300090274016

    • Pharmacological Class

    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]
    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]

    NDC Crossover Matching brand name "Depo-Medrol" or generic name "Methylprednisolone Acetate"

    NDCBrand NameGeneric Name
    0009-0274Depo-Medrolmethylprednisolone acetate
    0009-0280Depo-Medrolmethylprednisolone acetate
    0009-0306Depo-Medrolmethylprednisolone acetate
    0009-3073Depo-Medrolmethylprednisolone acetate
    0009-3475Depo-Medrolmethylprednisolone acetate
    70518-0516Depo-MedrolDepo-Medrol
    70518-1088Depo-MedrolDepo-Medrol
    21695-952Depo-MedrolDepo-Medrol
    50090-0312Depo-MedrolDepo-Medrol
    50090-1823Depo-MedrolDepo-Medrol
    50090-0556Depo-MedrolDepo-Medrol
    50090-2098Depo-MedrolDepo-Medrol
    55045-3243Depo-MedrolDepo-Medrol
    55154-3929Depo-MedrolDepo-Medrol
    55154-3932Depo-MedrolDepo-Medrol
    70518-2148Depo-MedrolDepo-Medrol
    76420-081Depo-MedrolDepo-Medrol
    50090-0436Depo-MedrolDepo-Medrol
    0703-0031Methylprednisolone AcetateMethylprednisolone Acetate
    0703-0043Methylprednisolone AcetateMethylprednisolone Acetate
    0703-0045Methylprednisolone AcetateMethylprednisolone Acetate

    Trademark Results [Depo-Medrol]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    DEPO-MEDROL
    DEPO-MEDROL
    72078585 0694836 Live/Registered
    UPJOHN COMPANY, THE
    1959-07-28
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