NDC 60760-964

Oxycodone Hydrochloride and Acetaminophen 325 mg / 7.5 mg tablet

On the label: St. Mary's Medical Park Pharmacy. It's repackaged: St. Mary's Medical Park Pharmacy rebottles it from Elite Laboratories, Inc.'s NDC 64850-622.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Elite Laboratories, Inc.Northvale, NJ, United StatesMakes it and labels it Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action

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 ANDA209385
On the market since
Oct 7, 2025
Package NDCs
60760-964-30 60760-964-60 60760-964-90
Official label
DailyMed (National Library of Medicine), updated Aug 14, 2026

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