NDC 68382-955

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients 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

Product details

Generic drug
Amphetamine and Dextroamphetamine: every company that makes it
Form
tablet
Strength
4 ingredients
Approval
ANDA ANDA207340
On the market since
Oct 31, 2017
Package NDCs
68382-955-01
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2020

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