NDC 0245-0410

Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet

On the label: Upsher-Smith Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it and packages it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
5 mg / 325 mg
Approval
ANDA ANDA206484
On the market since
Mar 27, 2017
Package NDCs
0245-0410-01 0245-0410-11 0245-0410-50 0245-0410-89
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2025

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