Oxaprozin

Product NDC

50436-2899

11-digit product format

504362899

Labeler code

50436

Product ID

50436-2899_04491d11-f854-4302-b297-1ff55ea22268

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxaprozin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA075849

Marketing category

ANDA

Marketing start

2003-05-12

Marketing end

0000-00-00

Substance

OXAPROZIN

Active strength

600 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record