71335-0610 NDC - OXYBUTYNIN CHLORIDE ()

Drug Information

Product NDC: 71335-0610

Proprietary Name: oxybutynin chloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	71335-0610-1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-1)
2	71335-0610-2	18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-2)
3	71335-0610-3	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-3)
4	71335-0610-4	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-4)

Field Name	Field Value	Definition
PRODUCT NDC	71335-0610	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	oxybutynin chloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	12/20/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Bryant Ranch Prepack	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024