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

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Atenolol

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING


DOSAGE AND ADMINISTRATION

ATENOLOL DESCRIPTION


Atenolol








CLINICAL PHARMACOLOGY



PHARMACOKINETICS

DOSAGE AND ADMINISTRATION

PHARMACODYNAMICS













INDICATIONS & USAGE

Hypertension


Angina Pectoris Due to Coronary Atherosclerosis


Acute Myocardial Infarction
DOSAGE AND ADMINISTRATIONCONTRAINDICATIONSWARNINGS

ATENOLOL CONTRAINDICATIONS

WARNINGS


WARNINGS

Cardiac Failure



In Patients Without a History of Cardiac Failure
DOSAGE AND ADMNISTRATION



DOSAGE AND ADMINISTRATION

Concomitant Use of Calcium Channel Blockers
PRECAUTIONS

Bronchospastic Diseases


Anesthesia and Major Surgery

OVERDOSAGE

Diabetes and Hypoglycemia


Thyrotoxicosis
DOSAGE AND ADMINISTRATION).

Untreated Pheochromocytoma


Pregnancy and Fetal Injury

PRECAUTIONS, Nursing Mothers



PRECAUTIONS

General


Impaired Renal Function
DOSAGE AND ADMINISTRATION

DRUG INTERACTIONS


WARNINGS








CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY




ANIMAL PHARMACOLOGY & OR TOXICOLOGY



PREGNANCY


WARNINGS - Pregnancy and Fetal Injury

NURSING MOTHERS


WARNINGS, Pregnancy and Fetal Injury

PEDIATRIC USE



GERIATRIC USE




CLINICAL PHARMACOLOGYINDICATIONS AND USAGE


ATENOLOL ADVERSE REACTIONS




WARNINGS
Acute Myocardial Infarction





Reasons for Reduced Dosage


POTENTIAL ADVERSE EFFECTS





INDICATIONS AND USAGE


OVERDOSAGE












DOSAGE & ADMINISTRATION

Hypertension



Angina Pectoris



Acute Myocardial Infarction






Elderly Patients or Patients with Renal Impairment







Cessation of Therapy in Patients with Angina Pectoris


HOW SUPPLIED

Atenolol Tablets, USP























PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Atenolol






Atenolol








Atenolol

Atenolol TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-176(NDC:63304-621)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ATENOLOL ATENOLOL 25 mg

Inactive Ingredients

Ingredient Name Strength
MAGNESIUM CARBONATE
MAGNESIUM STEARATE
SILICON DIOXIDE
SODIUM LAURYL SULFATE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
white 6 mm RE;19 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-176-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077877 2011-04-25


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