NDC 60760-382 – Oxaprozin

Oxaprozin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60760-382

Product details

Brand name
Oxaprozin
Generic name
Oxaprozin
Labeler
ST MARY'S MEDICAL PARK PHARMACY
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075855
Marketed since
August 15, 2022
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaprozin →

Package NDC codes (1)

Package NDCDescriptionSince
60760-382-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-382-14)Aug 15, 2022

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