NDC 71205-978 – Nabumetone

Nabumetone 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-978

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078420
Marketed since
September 25, 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 (6)

Package NDCDescriptionSince
71205-978-00100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00)May 7, 2020
71205-978-3030 TABLET in 1 BOTTLE, PLASTIC (71205-978-30)May 7, 2020
71205-978-55500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)May 7, 2020
71205-978-6060 TABLET in 1 BOTTLE, PLASTIC (71205-978-60)May 7, 2020
71205-978-72120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72)May 7, 2020
71205-978-9090 TABLET in 1 BOTTLE, PLASTIC (71205-978-90)May 7, 2020

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