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

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Amlodipine

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

AMLODIPINE DESCRIPTION


Amlodipine





CLINICAL PHARMACOLOGY

Mechanism of Action




Pharmacokinetics and Metabolism



Pediatric Patients


Pharmacodynamics



Clinical Studies




INDICATIONS & USAGE





AMLODIPINE CONTRAINDICATIONS



WARNINGS

Increased Angina and/or Myocardial Infarction


PRECAUTIONS



INFORMATION FOR PATIENTS

CLINICAL PHARMACOLOGY

Beta-Blocker Withdrawal


Patients with Hepatic Failure


DRUG INTERACTIONS



Effect of Other Agents on Amlodipine





Effect of Amlodipine on Other Agents






Drug/laboratory test interactions


CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



PREGNANCY

Category C:


NURSING MOTHERS



PEDIATRIC USE



GERIATRIC USE

DOSAGE AND ADMINISTRATION

AMLODIPINE ADVERSE REACTIONS



N=275 N=296 N=268 N=520


































OVERDOSAGE




DOSAGE & ADMINISTRATION

Adults

ADVERSE REACTIONS

Children
CLINICAL PHARMACOLOGY

Coadministration with Other Antihypertensive and/or AntianginalDrugs


SPL PATIENT PACKAGE INSERT







What is amlodipine besylate?















Who should not use amlodipine besylate?




What should I tell my doctor before taking amlodipine besylate?









How should I take amlodipine besylate?



















What should I avoid while taking amlodipine besylate?





What are the possible side effects of amlodipine besylate?

















How do I store amlodipine besylate?





General advice about amlodipine besylate





PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Amlodipine



Amlodipine



Amlodipine

Amlodipine TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-160(NDC:60505-0195-3)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
amlodipine besylate AMLODIPINE 10 mg

Inactive Ingredients

Ingredient Name Strength
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
BUTYLATED HYDROXYTOLUENE
cellulose, microcrystalline
SODIUM STARCH GLYCOLATE TYPE A POTATO
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 10 mm APO;AML;10 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-160-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076719 2011-04-13


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Be sure to consult your doctor before taking any medication!
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