NDC 55648-101

Bupropion Hydrochloride(SR) 100 mg tablet, film coated, extended release

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
Bupropion: every company that makes it
Form
tablet, film coated, extended release
Strength
100 mg
Approval
ANDA ANDA201331
On the market since
Aug 30, 2012
Package NDCs
55648-101-01 55648-101-02 55648-101-03 55648-101-05 55648-101-07 55648-101-08
Official label
DailyMed (National Library of Medicine), updated Nov 6, 2012

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