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

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Hydralazine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

HYDRALAZINE HYDROCHLORIDE DESCRIPTION


Hydralazine Hydrochloride





CLINICAL PHARMACOLOGY





INDICATIONS & USAGE



HYDRALAZINE HYDROCHLORIDE CONTRAINDICATIONS



WARNINGS

PRECAUTIONSLaboratory Tests

PRECAUTIONS

General:





INFORMATION FOR PATIENTS



LABORATORY TESTS





DRUG INTERACTIONS




Drug/Food Interactions:


CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY




PREGNANCY

Category C:



NURSING MOTHERS



PEDIATRIC USE



HYDRALAZINE HYDROCHLORIDE ADVERSE REACTIONS


Common:
Less Frequent:Digestive:
  • ●     Cardiovascular: hypotension, paradoxical pressor response, edema.
  • ●     Respiratory: dyspnea
  • ●     Neurologic: peripheral neuritis, evidenced by paresthesia, numbness, and tingling; dizziness; tremors; muscle cramps; psychotic reactions characterized by depression, disorientation, or anxiety.
  • ●     Genitourinary: difficulty in urination
  • ●     Hematologic: blood dyscrasias, consisting of reduction in hemoglobin and red cell count, leukopenia, agranulocytosis, purpura; lymphadenopathy; splenomegaly.
  • ●     Hypersensitivity Reactions: rash, urticaria, pruritus, fever, chills, arthralgia, eosinophilia, and rarely, hepatitis.
  • ●     Other: nasal congestion, flushing, lacrimation, conjunctivitis.

OVERDOSAGE

Acute Toxicity:



Treatment:





DOSAGE & ADMINISTRATION





HOW SUPPLIED







STORAGE AND HANDLING




PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Hydralazine Hydrochloride

Hydralazine Hydrochloride

Hydralazine Hydrochloride

Hydralazine Hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-819(NDC:31722-519)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYDRALAZINE HYDROCHLORIDE HYDRALAZINE 10 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS LACTOSE
cellulose, microcrystalline
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID
FD&C YELLOW NO. 6

Product Characteristics

Color Size Imprint Code Shape
orange 5 mm H;38 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-819-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040901 2011-11-17


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