NDC 52959-800

Oxaprozin 600 mg tablet, film coated

On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-170.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Dr. Reddy's Laboratories LimitedMedchal-Malkajgiri, IndiaMakes it and tests it Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections

Product details

Generic drug
Oxaprozin: every company that makes it
Form
tablet, film coated
Strength
600 mg
Approval
ANDA ANDA075855
On the market since
Jan 31, 2001
Package NDCs
52959-800-00 52959-800-14 52959-800-15 52959-800-20 52959-800-21 52959-800-24 52959-800-28 52959-800-30 52959-800-40 52959-800-42 52959-800-45 52959-800-60
Official label
DailyMed (National Library of Medicine), updated Oct 14, 2011

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