NDC 55648-991

Ziprasidone hydrochloride 20 mg capsule

On the label: Wockhardt Limited.

Where it's made

FactoryWhereRoleLast FDA inspection
Wockhardt LimitedLocation not on fileMakes it, tests it, packages it and labels it Not inspected on record

Product details

Generic drug
Ziprasidone: every company that makes it
Form
capsule
Strength
20 mg
Approval
ANDA ANDA090348
On the market since
Sep 1, 2012
Package NDCs
55648-991-01 55648-991-02 55648-991-03 55648-991-04 55648-991-06
Official label
DailyMed (National Library of Medicine), updated Jul 20, 2012

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