NDC 52959-300

Cefprozil 500 mg tablet

On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-404.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lupin LimitedMandideep, IndiaMakes it, makes the active ingredient and packages it Serious problems, FDA actionNov 23, 2022 · 6 inspections, 3 with FDA action

Product details

Generic drug
Cefprozil: every company that makes it
Form
tablet
Strength
500 mg
Approval
ANDA ANDA065276
On the market since
Dec 8, 2005
Package NDCs
52959-300-20
Official label
DailyMed (National Library of Medicine), updated Nov 15, 2011

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