NDC 70934-529

Oxybutynin Chloride 5 mg tablet

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from ANI Pharmaceuticals, Inc.'s NDC 70954-005.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Repackaging site

Product details

Generic drug
Oxybutynin: every company that makes it
Form
tablet
Strength
5 mg
Approval
ANDA ANDA209823
On the market since
Jan 30, 2020
Package NDCs
70934-529-30 70934-529-60
Official label
DailyMed (National Library of Medicine), updated Jan 30, 2020

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