Oxaprozin

Product NDC

50090-2012

11-digit product format

500902012

Labeler code

50090

Product ID

50090-2012_ba37a5ed-24a7-42e5-af91-08ea707ac752

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxaprozin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA075855

Marketing category

ANDA

Marketing start

2001-01-31

Marketing end

0000-00-00

Substance

OXAPROZIN

Active strength

600 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record