NDC 72189-130

Oxybutynin Chloride 5 mg tablet

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-456.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.

Repackaging site

Product details

Generic drug
Oxybutynin: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA071655
On the market since
Nov 11, 2020
Package NDCs
72189-130-30
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?