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

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Hydrochlorothiazide

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

HYDROCHLOROTHIAZIDE DESCRIPTION


Hydrochlorothiazide




CLINICAL PHARMACOLOGY






PHARMACOKINETICS



INDICATIONS & USAGE





Use in Pregnancy

PRECAUTIONS, Pregnancy

HYDROCHLOROTHIAZIDE CONTRAINDICATIONS

CONTRAINDICATIONS



WARNINGS

WARNINGS




PRECAUTIONS, Drug lnteractions

PRECAUTIONS

General









LABORATORY TESTS

Laboratory Tests


DRUG INTERACTIONS

Drug Interactions




















DRUG & OR LABORATORY TEST INTERACTIONS

Drug/Laboratory Test Interactions
PRECAUTIONS, General

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY

Carcinogenesis, Mutagenesis, Impairment of Fertility




PREGNANCY

Teratogenic Effects




Nonteratogenic Effects


NURSING MOTHERS

Nursing Mothers


PEDIATRIC USE

Pediatric Use
DOSAGE AND ADMINISTRATION, Infants and Children

HYDROCHLOROTHIAZIDE ADVERSE REACTIONS

ADVERSE REACTIONS












PRECAUTIONS





WARNINGS








OVERDOSAGE

OVERDOSAGE




DOSAGE & ADMINISTRATION

DOSAGE AND ADMINISTRATION


Adults



PRECAUTIONS


Infants and Children

PRECAUTIONS, Pediatric Use

HOW SUPPLIED










INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
LACTOSE MONOHYDRATE

CELLULOSE, MICROCRYSTALLINE
FD&C YELLOW NO. 6
D&C YELLOW NO. 10
COLLOIDAL SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
MAGNESIUM STEARATE
ALUMINUM OXIDE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Hydrochlorothiazide



Hydrochlorothiazide




PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION













Hydrochlorothiazide


Hydrochlorothiazide

Hydrochlorothiazide TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-266(NDC:0527-1413)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE 25 mg

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
cellulose, microcrystalline
FD&C YELLOW NO. 6
D&C YELLOW NO. 10
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
MAGNESIUM STEARATE
ALUMINUM OXIDE

Product Characteristics

Color Size Imprint Code Shape
orange 6 mm LCI;1413 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-266-02 30 in 1 BLISTER PACK
2 NDC:49349-266-33 1000 in 1 CANISTER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084325 2011-05-09


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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