NDC 55648-743

Terbinafine Hydrochloride 250 mg tablet

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
Terbinafine: every company that makes it
Form
tablet
Strength
250 mg
Approval
ANDA ANDA078229
On the market since
Jul 2, 2007
Package NDCs
55648-743-01 55648-743-02 55648-743-03 55648-743-05
Official label
DailyMed (National Library of Medicine), updated Sep 7, 2012

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