NDC 80425-0053 – Nabumetone

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

Human Prescription Drug

Product NDC80425-0053

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078671
Marketed since
March 6, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (1)

Package NDCDescriptionSince
80425-0053-160 TABLET, FILM COATED in 1 BOTTLE (80425-0053-1)Mar 6, 2019

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