NDC 70934-065

Cephalexin 500 mg capsule

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-122.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lupin LimitedMandideep, IndiaMakes it Serious problems, FDA actionNov 23, 2022 · 6 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Cephalexin: every company that makes it
Form
capsule
Strength
500 mg
Approval
ANDA ANDA065229
On the market since
Jan 18, 2018
Package NDCs
70934-065-10 70934-065-14 70934-065-20 70934-065-21 70934-065-28 70934-065-30 70934-065-40 70934-065-94
Official label
DailyMed (National Library of Medicine), updated Mar 18, 2020

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