NDC 72189-191

Hydrocodone Bitartrate And Acetaminophen 325 mg / 7.5 mg tablet

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from KVK-TECH, Inc.'s NDC 10702-190.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA209037
On the market since
Sep 15, 2021
Package NDCs
72189-191-30
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2025

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