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FDA Drug information

Methylprednisolone

Read time: 1 mins
Marketing start date: 25 Jul 2024

Summary of product characteristics


Effective Time

20221031

Version

5

Spl Product Data Elements

methylprednisolone methylprednisolone METHYLPREDNISOLONE METHYLPREDNISOLONE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN WHITE TO OFF-WHITE OVAL 916 methylprednisolone methylprednisolone METHYLPREDNISOLONE METHYLPREDNISOLONE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN WHITE TO OFF-WHITE OVAL 917 methylprednisolone methylprednisolone METHYLPREDNISOLONE METHYLPREDNISOLONE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN WHITE TO OFF-WHITE OVAL 918 methylprednisolone methylprednisolone METHYLPREDNISOLONE METHYLPREDNISOLONE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO STARCH, CORN WHITE TO OFF-WHITE OVAL 919

Application Number

ANDA206751

Brand Name

Methylprednisolone

Generic Name

methylprednisolone

Product Ndc

70771-1349

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1348-1 in bottle of 100 tablets Methylprednisolone tablets, USP R x only 100 tablets NDC 70771-1349-8 in bottle of 25 tablets Methylprednisolone tablets, USP R x only 25 tablets NDC 70771-1350-7 in bottle of 50 tablets Methylprednisolone tablets, USP R x only 50 tablets NDC 70771-1351-8 in bottle of 25 tablets Methylprednisolone tablets, USP R x only 25 tablets methylprednisolone tablets methylprednisolone tablets methylprednisolone tablets methylprednisolone tablets

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