Clonidine Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Clonidine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

CLONIDINE HYDROCHLORIDE DESCRIPTION




Clonidine Hydrochloride




CLINICAL PHARMACOLOGY







PHARMACOKINETICS



INDICATIONS & USAGE



CLONIDINE HYDROCHLORIDE CONTRAINDICATIONS

PRECAUTIONS

WARNINGS

Withdrawal




PRECAUTIONS

General




Perioperative Use


INFORMATION FOR PATIENTS





DRUG INTERACTIONS



Toxicology

Toxicology




CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY

Carcinogenesis, Mutagenesis, Impairment of Fertility



PREGNANCY





NURSING MOTHERS



PEDIATRIC USE

Pediatric Use
WARNINGS, Withdrawal

CLONIDINE HYDROCHLORIDE ADVERSE REACTIONS















OVERDOSAGE







DOSAGE & ADMINISTRATION

Adults


Initial Dose


Maintenance Dose



Renal Impairment


HOW SUPPLIED























PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Clonidine Hydrochloride

Clonidine Hydrochloride

Clonidine Hydrochloride

Clonidine Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-252(NDC:53489-216)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CLONIDINE HYDROCHLORIDE clonidine 0.2 mg

Inactive Ingredients

Ingredient Name Strength
AMMONIUM CHLORIDE
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
cellulose, microcrystalline
SODIUM LAURYL SULFATE

Product Characteristics

Color Size Imprint Code Shape
white 7 mm MP;658 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-252-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070924 2011-03-28


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Be sure to consult your doctor before taking any medication!
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