NDC 76420-322

Oxycodone And Acetaminophen 325 mg / 7.5 mg tablet

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-950.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Oxycodone: every company that makes it
Form
tablet, oral
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA207419
On the market since
Apr 11, 2017
Package NDCs
76420-322-01 76420-322-05 76420-322-30 76420-322-60 76420-322-90
Official label
DailyMed (National Library of Medicine), updated Apr 15, 2025

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