NDC 71205-030 – Nabumetone

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

Human Prescription Drug

Product NDC71205-030

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Proficient Rx LP
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 (4)

Package NDCDescriptionSince
71205-030-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-20)Jan 19, 2022
71205-030-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-30)May 1, 2018
71205-030-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-60)May 1, 2018
71205-030-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-90)May 1, 2018

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