Home – Hydralazine Hydrochloride
Hydralazine Hydrochloride
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
HYDRALAZINE HYDROCHLORIDE DESCRIPTION
INACTIVE INGREDIENT
CLINICAL PHARMACOLOGY
INDICATIONS & USAGE
HYDRALAZINE HYDROCHLORIDE CONTRAINDICATIONS
CONTRAINDICATIONS
WARNINGS
PRECAUTIONS, Laboratory TestsPRECAUTIONS
General
INFORMATION FOR PATIENTS
LABORATORY TESTS
DRUG INTERACTIONS
Drug/Food Interactions
CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY
Carcinogenesis, Mutagenesis, Impairment of Fertility
PREGNANCY
NURSING MOTHERS
PEDIATRIC USE
HYDRALAZINE HYDROCHLORIDE ADVERSE REACTIONS
OVERDOSAGE
OVERDOSAGE
DOSAGE & ADMINISTRATION
HOW SUPPLIED
STORAGE AND HANDLING
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
Hydralazine Hydrochloride
Hydralazine Hydrochloride TABLET, FILM COATED
Product Information
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Product Type
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Human prescription drug label |
Item Code (Source)
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NDC:49349-229(NDC:23155-002) |
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Route of Administration
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ORAL |
DEA Schedule
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Product Characteristics
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Color
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Size
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Imprint Code
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Shape
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pink |
8 mm |
HP;2 |
ROUND |
Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:49349-229-02 |
30 in 1 BLISTER PACK |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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ANDA |
ANDA086242 |
2011-04-28 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
