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

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Diltiazem Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DILTIAZEM HYDROCHLORIDE DESCRIPTION


Diltiazem Hydrochloride











CLINICAL PHARMACOLOGY









WARNINGS

PHARMACOKINETICS AND METABOLISM



INDICATIONS & USAGE




DILTIAZEM HYDROCHLORIDE CONTRAINDICATIONS



PRECAUTIONS

General

ADVERSE REACTIONS

DRUG INTERACTIONS

WARNINGSWARNINGS


WARNINGS

WARNINGS





CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



PREGNANCY




NURSING MOTHERS



PEDIATRIC USE



DILTIAZEM HYDROCHLORIDE ADVERSE REACTIONS
















OVERDOSAGE












DOSAGE & ADMINISTRATION






WARNINGSPRECAUTIONS


WARNINGS

ADVERSE REACTIONS


PRECAUTIONS

HOW SUPPLIED


















PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Diltiazem Hydrochloride



Diltiazem Hydrochloride



Diltiazem Hydrochloride

Diltiazem Hydrochloride CAPSULE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-003(NDC:0228-2577)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE DILTIAZEM 180 mg

Inactive Ingredients

Ingredient Name Strength
AMMONIO METHACRYLATE COPOLYMER TYPE A
AMMONIO METHACRYLATE COPOLYMER TYPE B
ACETYLCARNITINE, DL-
D&C YELLOW NO. 10
GELATIN
hydroxypropyl cellulose
PHENOXYISOPROPANOL
SILICON DIOXIDE
DIMETHICONE 410
SODIUM LAURYL SULFATE
talc
titanium dioxide
ACETYLTRIETHYL CITRATE
FD&C BLUE NO. 1
FD&C GREEN NO. 3

Product Characteristics

Color Size Imprint Code Shape
blue 22 mm R2577 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-003-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074984 2011-08-03


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