NDC 68071-1792

SOLU-MEDROL

Methylprednisolone Sodium Succinate

SOLU-MEDROL is a Intramuscular; Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals,inc.. The primary component is Methylprednisolone Sodium Succinate.

Product ID68071-1792_7df1b93e-74a2-aada-e053-2991aa0a6e99
NDC68071-1792
Product TypeHuman Prescription Drug
Proprietary NameSOLU-MEDROL
Generic NameMethylprednisolone Sodium Succinate
Dosage FormInjection, Powder, For Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date1959-04-02
Marketing CategoryNDA / NDA
Application NumberNDA011856
Labeler NameNuCare Pharmaceuticals,Inc.
Substance NameMETHYLPREDNISOLONE SODIUM SUCCINATE
Active Ingredient Strength125 mg/2mL
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68071-1792-2

2 mL in 1 BOTTLE, GLASS (68071-1792-2)
Marketing Start Date2018-05-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-1792-2 [68071179202]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION
Marketing CategoryNDA
Application NumberNDA011856
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-04

Drug Details

Active Ingredients

IngredientStrength
METHYLPREDNISOLONE SODIUM SUCCINATE125 mg/2mL

OpenFDA Data

SPL SET ID:6b64e2f0-0b08-200d-e053-2991aa0a220c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1743704
  • 1743707
  • Pharmacological Class

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

    NDC Crossover Matching brand name "SOLU-MEDROL" or generic name "Methylprednisolone Sodium Succinate"

    NDCBrand NameGeneric Name
    0009-0003SOLU-MEDROLmethylprednisolone sodium succinate
    0009-0018SOLU-MEDROLmethylprednisolone sodium succinate
    0009-0039SOLU-MEDROLmethylprednisolone sodium succinate
    0009-0047SOLU-MEDROLmethylprednisolone sodium succinate
    0009-0698SOLU-MEDROLmethylprednisolone sodium succinate
    68071-1792SOLU-MEDROLSOLU-MEDROL
    70385-2016SOLU-MEDROLSOLU-MEDROL
    70518-0334SOLU-MEDROLSOLU-MEDROL
    70518-1424SOLU-MEDROLSOLU-MEDROL
    71872-7061SOLU-MEDROLSOLU-MEDROL
    0009-0758SOLU-MEDROLSOLU-MEDROL
    0009-0796Solu-MedrolSolu-Medrol
    50090-0271SOLU-MEDROLSOLU-MEDROL
    51662-1263SOLU-MEDROLSOLU-MEDROL
    51662-1264SOLU-MEDROLSOLU-MEDROL
    52584-039Solu-MedrolSolu-Medrol
    52584-047Solu-MedrolSolu-Medrol
    55154-3939Solu-MedrolSolu-Medrol
    55154-3941Solu-MedrolSolu-Medrol
    55154-3940Solu-MedrolSolu-Medrol
    55154-3944Solu-MedrolSolu-Medrol
    61699-0047SOLU-MEDROLSOLU-MEDROL
    70518-2023SOLU-MEDROLSOLU-MEDROL
    0009-0850SOLU-MEDROLSOLU-MEDROL

    Trademark Results [SOLU-MEDROL]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    SOLU-MEDROL
    SOLU-MEDROL
    85620834 4264329 Live/Registered
    Pharmacia & UpJohn Company LLC
    2012-05-09
    SOLU-MEDROL
    SOLU-MEDROL
    72057303 0676234 Dead/Cancelled
    UPJOHN COMPANY, THE
    1958-08-15

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.