NDC 43063-972 – Nabumetone

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

Human Prescription Drug

Product NDC43063-972

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (2)

Package NDCDescriptionSince
43063-972-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)Apr 22, 2019
43063-972-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)Jul 10, 2019

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