NDC 67296-1705

Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-942.

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 Hydrocodone: every company that makes it
Form
tablet
Strength
325 mg / 7.5 mg
Approval
ANDA ANDA211487
On the market since
Nov 1, 2019
Package NDCs
67296-1705-3 67296-1705-6
Official label
DailyMed (National Library of Medicine), updated Aug 2, 2024

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