Oxybutynin Chloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Oxybutynin Chloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OXYBUTYNIN CHLORIDE DESCRIPTION


Oxybutynin Chloride








CLINICAL PHARMACOLOGY





PHARMACOKINETICS






Oxybutynin Chloride





**Oxybutynin Chloride



Food Effects


Distribution


Metabolism


Excretion


CLINICAL STUDIES



INDICATIONS & USAGE



OXYBUTYNIN CHLORIDE CONTRAINDICATIONS




WARNINGS



PRECAUTIONS

Central Nervous System Effects
ADVERSE REACTIONS


General



Urinary Retention
CONTRAINDICATIONS

Gastrointestinal Disorders
CONTRAINDICATIONS




INFORMATION FOR PATIENTS






DRUG INTERACTIONS






CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY





PREGNANCY



NURSING MOTHERS



PEDIATRIC USE

DOSAGE AND ADMINISTRATION




GERIATRIC USE



OXYBUTYNIN CHLORIDE ADVERSE REACTIONS







Postmarketing Surveillance


OVERDOSAGE





DOSAGE & ADMINISTRATION




HOW SUPPLIED




STORAGE AND HANDLING





REFERENCES








PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Oxybutynin Chloride

Oxybutynin Chloride

Oxybutynin Chloride

Oxybutynin Chloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-545(NDC:50111-456)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OXYBUTYNIN CHLORIDE OXYBUTYNIN 5 mg

Inactive Ingredients

Ingredient Name Strength
CALCIUM STEARATE
cellulose, microcrystalline
ANHYDROUS LACTOSE
SODIUM STARCH GLYCOLATE TYPE A POTATO
FD&C BLUE NO. 1
ALUMINUM OXIDE

Product Characteristics

Color Size Imprint Code Shape
blue 8 mm PLIVA;456 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-545-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA071655 2011-09-29


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