Home – Clonidine Hydrochloride
Clonidine Hydrochloride
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
CLONIDINE HYDROCHLORIDE DESCRIPTION
CLINICAL PHARMACOLOGY
Pharmacokinetics:INDICATIONS & USAGE
CLONIDINE HYDROCHLORIDE CONTRAINDICATIONS
PRECAUTIONSWARNINGS
PRECAUTIONS
General
INFORMATION FOR PATIENTS
DRUG INTERACTIONS
ToxicologyCARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY
USE IN SPECIFIC POPULATIONS
Teratogenic Effects
NURSING MOTHERS
PEDIATRIC USE
WARNINGSWithdrawalCLONIDINE HYDROCHLORIDE ADVERSE REACTIONS
OVERDOSAGE
DOSAGE & ADMINISTRATION
HOW SUPPLIED
STORAGE AND HANDLING
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
Clonidine Hydrochloride
Clonidine Hydrochloride 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:49349-445(NDC:0228-2127) |
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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
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CLONIDINE HYDROCHLORIDE clonidine |
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0.1 mg
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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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orange |
6 mm |
R127 |
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:49349-445-02 |
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 |
ANDA070974 |
2011-08-01 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
