NDC 67296-1333

Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-201.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Knoa Pharmaceuticals LLCWilson, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 9 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet
Strength
5 mg / 325 mg
Approval
ANDA ANDA202991
On the market since
Apr 12, 2016
Package NDCs
67296-1333-0 67296-1333-1 67296-1333-2 67296-1333-3 67296-1333-4 67296-1333-5 67296-1333-6 67296-1333-7 67296-1333-8 67296-1333-9
Official label
DailyMed (National Library of Medicine), updated Jan 20, 2022

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