NDC 71335-1391 – Nabumetone

Nabumetone 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1391

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078420
Marketed since
June 26, 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 (9)

Package NDCDescriptionSince
71335-1391-120 TABLET in 1 BOTTLE (71335-1391-1)Dec 9, 2019
71335-1391-230 TABLET in 1 BOTTLE (71335-1391-2)Dec 20, 2019
71335-1391-360 TABLET in 1 BOTTLE (71335-1391-3)Nov 14, 2019
71335-1391-490 TABLET in 1 BOTTLE (71335-1391-4)Nov 7, 2019
71335-1391-542 TABLET in 1 BOTTLE (71335-1391-5)Dec 28, 2021
71335-1391-656 TABLET in 1 BOTTLE (71335-1391-6)Jul 13, 2020
71335-1391-714 TABLET in 1 BOTTLE (71335-1391-7)Dec 28, 2021
71335-1391-8100 TABLET in 1 BOTTLE (71335-1391-8)Dec 28, 2021
71335-1391-99 TABLET in 1 BOTTLE (71335-1391-9)Dec 28, 2021

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