NDC 76282-257 – Nabumetone

Nabumetone 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC76282-257

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078671
Marketed since
April 14, 2015
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (2)

Package NDCDescriptionSince
76282-257-01100 TABLET, FILM COATED in 1 BOTTLE (76282-257-01)Apr 14, 2015
76282-257-05500 TABLET, FILM COATED in 1 BOTTLE (76282-257-05)Apr 14, 2015

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