Home – Ranitidine Hydrochloride
Ranitidine Hydrochloride
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
RANITIDINE HYDROCHLORIDE DESCRIPTION
CLINICAL PHARMACOLOGY
PHARMACOKINETICS
PHARMACODYNAMICS
PHARMACODYNAMICS
INDICATIONS & USAGE
RANITIDINE HYDROCHLORIDE CONTRAINDICATIONS
PRECAUTIONS
LABORATORY TESTS
LABORATORY TESTS
DRUG INTERACTIONS
CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY
CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY
PREGNANCY
NURSING MOTHERS
PEDIATRIC USE
PEDIATRIC USE
GERIATRIC USE
GERIATRIC USE
RANITIDINE HYDROCHLORIDE ADVERSE REACTIONS
ADVERSE REACTIONS
OVERDOSAGE
OVERDOSAGE
DOSAGE & ADMINISTRATION
DOSAGE & ADMINISTRATION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
Ranitidine Hydrochloride
Ranitidine Hydrochloride TABLET
Product Information
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Product Type
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Human prescription drug label |
Item Code (Source)
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NDC:49349-165(NDC:60505-0025-8) |
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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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white |
8 mm |
RAN;150;APO |
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:49349-165-02 |
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 |
ANDA074680 |
2011-04-14 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
