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NDC 10702-0201-10

Oxybutynin Chloride 5 mg/1 TABLET

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NDC
10702-0201-10
Generic Name
Oxybutynin Chloride
Brand Name
Oxybutynin Chloride
Strength
5 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
KVK-Tech, Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Oxybutynin chloride is indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

Important Warnings

WARNINGS Angioedema of the face, lips, tongue and/or larynx has been reported with oxybutynin. In some cases, angioedema occurred after the first dose. Angioedema associated with upper airway swelling may be life-threatening. If involvement of the tongue, hypopharynx, or larynx occurs, oxybutynin should be promptly discontinued and appropriate therapy and/or measures necessary to ensure a patent a…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Oxybutynin Chloride NDC Codes

64380-0162-025 mg/1TABLET
2-Day
64380-0162-035 mg/1TABLET
2-Day
16729-0317-015 mg/1TABLET, EXTENDED RELEASE
2-Day
64380-0162-015 mg/1TABLET
2-Day

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