Hydrocodone Bitartrate and Acetaminophen description, usages, side effects, indications, overdosage, supplying and lots more!

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Hydrocodone Bitartrate and Acetaminophen

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

HYDROCODONE BITARTRATE AND ACETAMINOPHEN DESCRIPTION



Hydrocodone Bitartrate and Acetaminophen



Hydrocodone Bitartrate and Acetaminophen








CLINICAL PHARMACOLOGY




PHARMACOKINETICS



OVERDOSAGE
OVERDOSAGE

INDICATIONS & USAGE

INDICATIONS AND USAGE


HYDROCODONE BITARTRATE AND ACETAMINOPHEN CONTRAINDICATIONS

CONTRAINDICATIONS



WARNINGS

WARNINGS

Respiratory Depression


Head Injury and Increased Intracranial Pressure


Acute Abdominal Conditions


Misuse, Abuse, and Diversion of Opioids

DRUG ABUSE AND DEPENDENCE

PRECAUTIONS

General



INFORMATION FOR PATIENTS





LABORATORY TESTS

Laboratory Tests


DRUG INTERACTIONS

Drug Interactions



DRUG & OR LABORATORY TEST INTERACTIONS

Drug/Laboratory Test Interactions


CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY

Carcinogenesis, Mutagenesis, Impairment of Fertility




LABOR & DELIVERY

Labor and Delivery


NURSING MOTHERS

Nursing Mothers


PEDIATRIC USE

Pediatric Use


GERIATRIC USE

Geriatric Use




HYDROCODONE BITARTRATE AND ACETAMINOPHEN ADVERSE REACTIONS

ADVERSE REACTIONS





OVERDOSAGE




DRUG ABUSE AND DEPENDENCE

DRUG ABUSE AND DEPENDENCE

Misuse, Abuse, and Diversion of Opioids






OVERDOSAGE

OVERDOSAGE


Signs and Symptoms













DOSAGE & ADMINISTRATION




STORAGE AND HANDLING





INACTIVE INGREDIENT

SILICON DIOXIDE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate and Acetaminophen TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-636(NDC:0591-0388-01)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYDROCODONE BITARTRATE HYDROCODONE 2.5 mg
ACETAMINOPHEN ACETAMINOPHEN 500 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
MAGNESIUM STEARATE
cellulose, microcrystalline

Product Characteristics

Color Size Imprint Code Shape
white 17 mm 388 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-636-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040123 2011-04-08


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Be sure to consult your doctor before taking any medication!
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