Prednisone
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
PREDNISONE DESCRIPTION
CLINICAL PHARMACOLOGY
INDICATIONS & USAGE
PREDNISONE CONTRAINDICATIONS
WARNINGS
PRECAUTIONS
General
DOSAGE AND ADMINISTRATIONINFORMATION FOR PATIENTS
PREDNISONE ADVERSE REACTIONS
DOSAGE & ADMINISTRATION
Multiple Sclerosis
ADT(Alternate Day Therapy)
HOW SUPPLIED
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
Prednisone
Prednisone TABLET
Product Information
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Product Type
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Human prescription drug label |
Item Code (Source)
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NDC:49349-717(NDC:0603-5338) |
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Route of Administration
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ORAL |
DEA Schedule
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Active Ingredient/Active Moiety
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Ingredient Name
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Basis of Strength
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Strength
|
|
PREDNISONE PREDNISONE |
|
10 mg
|
Product Characteristics
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Color
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Size
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Imprint Code
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Shape
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white |
9 mm |
5093;V |
ROUND |
Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:49349-717-02 |
30 in 1 BLISTER PACK |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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|
ANDA |
ANDA040256 |
2011-08-30 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
