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

Clonidine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DESCRIPTION




DESCRIPTION



CLINICAL PHARMACOLOGY






Pharmacokinetics:

INDICATIONS & USAGE



CONTRAINDICATIONS

PRECAUTIONS

WARNINGS

Withdrawal:

Because children commonly have gastrointestinal illnesses that lead to vomiting, they may be particularly susceptible to hypertensive episodes resulting from abrupt inability to take medication.

PRECAUTIONS

General



Perioperative Use:

INFORMATION FOR PATIENTS




DRUG INTERACTIONS



Toxicology
Toxicology:



CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY




PREGNANCY

Teratogenic Effects




NURSING MOTHERS



PEDIATRIC USE

WARNINGSWithdrawal

ADVERSE REACTIONS















OVERDOSAGE





DOSAGE & ADMINISTRATION






HOW SUPPLIED











PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

Clonidine Hydrochloride

Clonidine Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-434(NDC:0228-2128)
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
lactose monohydrate
MAGNESIUM STEARATE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
D&C YELLOW NO. 10
FD&C YELLOW NO. 6

Product Characteristics

Color Size Imprint Code Shape
orange 7 mm R128 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-434-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070975 2011-07-29


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Be sure to consult your doctor before taking any medication!
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