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

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Benazepril Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING

USE IN PREGNANCY


BENAZEPRIL HYDROCHLORIDE DESCRIPTION


Benazepril Hydrochloride





CLINICAL PHARMACOLOGY

Mechanism of Action






PHARMACOKINETICS

Pharmacokinetics and Metabolism












PHARMACODYNAMICS



Hypertension

Adult









Pediatrics


INDICATIONS & USAGE





BENAZEPRIL HYDROCHLORIDE CONTRAINDICATIONS



WARNINGS

Anaphylactoid and Possibly Related Reactions


Head and Neck Angioedema


Intestinal Angioedema


Anaphylactoid Reactions During Desensitization


Anaphylactoid Reactions During Membrane Exposure


Hypotension




Neutropenia/Agranulocytosis


Fetal/Neonatal Morbidity and Mortality








Hepatic Failure


PRECAUTIONS

General

Impaired Renal Function


Hyperkalemia


Cough


Impaired Liver Function


Surgery/Anesthesia


INFORMATION FOR PATIENTS

Pregnancy


Angioedema


Symptomatic Hypotension



Hyperkalemia


Neutropenia


DRUG INTERACTIONS

Diuretics


Potassium Supplements and Potassium-Sparing Diuretics


Oral Anticoagulants


Lithium


Gold


Anti-Diabetics


Other



CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



PREGNANCY



NURSING MOTHERS



GERIATRIC USE




PEDIATRIC USE




BENAZEPRIL HYDROCHLORIDE ADVERSE REACTIONS









Cardiovascular


Renal


Fetal/Neonatal Morbidity and Mortality


Angioedema


Dermatologic


Gastrointestinal


Hematologic


Neurologic and Psychiatric


Other




Pediatric Patients



Clinical Laboratory Test Findings

Creatinine and Blood Urea Nitrogen


Potassium


Hemoglobin


Other (Causal Relationships Unknown)


OVERDOSAGE






DOSAGE & ADMINISTRATION

Hypertension

Adults






Pediatrics




For Hypertensive Patients with Renal Impairment


Preparation of Suspension (for 150 mL of a 2.0 mg/mL suspension)



HOW SUPPLIED






STORAGE AND HANDLING




PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Benazepril Hydrochloride

Benazepril Hydrochloride

Benazepril Hydrochloride

Benazepril Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-302(NDC:0093-5126)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENAZEPRIL HYDROCHLORIDE BENAZEPRILAT 20 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
CROSPOVIDONE
HYPROMELLOSES
FERRIC OXIDE YELLOW
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol
povidone
STARCH, CORN
titanium dioxide
triacetin
FERROSOFERRIC OXIDE
ferric oxide red

Product Characteristics

Color Size Imprint Code Shape
pink 8 mm 93;5126 TRIANGLE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-302-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076211 2011-06-16


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Be sure to consult your doctor before taking any medication!
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