NDC 71335-1234 – Nabumetone

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

Human Prescription Drug

Product NDC71335-1234

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091083
Marketed since
June 13, 2011
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1234-120 TABLET, FILM COATED in 1 BOTTLE (71335-1234-1)May 29, 2019
71335-1234-230 TABLET, FILM COATED in 1 BOTTLE (71335-1234-2)Oct 22, 2019
71335-1234-360 TABLET, FILM COATED in 1 BOTTLE (71335-1234-3)Jul 3, 2019
71335-1234-490 TABLET, FILM COATED in 1 BOTTLE (71335-1234-4)Jun 19, 2019
71335-1234-542 TABLET, FILM COATED in 1 BOTTLE (71335-1234-5)May 2, 2022
71335-1234-656 TABLET, FILM COATED in 1 BOTTLE (71335-1234-6)Jul 15, 2019
71335-1234-714 TABLET, FILM COATED in 1 BOTTLE (71335-1234-7)May 2, 2022
71335-1234-8100 TABLET, FILM COATED in 1 BOTTLE (71335-1234-8)May 2, 2022
71335-1234-99 TABLET, FILM COATED in 1 BOTTLE (71335-1234-9)May 2, 2022

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