NDC 68382-796

Oxycodone Hydrochloride 20 mg tablet

On the label: Zydus Pharmaceuticals (USA) Inc..

Where it's made

FactoryWhereRoleLast FDA inspection
Nesher Pharmaceuticals (USA) LLCLocation not on fileMakes it and tests it Not inspected on record
Nesher Pharmaceuticals (USA) LLCLocation not on fileMakes it Not inspected on record

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet
Strength
20 mg
Approval
ANDA ANDA077290
On the market since
Dec 26, 2012
Package NDCs
68382-796-01
Official label
DailyMed (National Library of Medicine), updated Dec 17, 2021

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