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NDC 72189-0184-90 NABUMETONE 500 mg/1 Details

NABUMETONE 500 mg/1

NABUMETONE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by direct rx. The primary component is NABUMETONE.

MedlinePlus Drug Summary

Nabumetone is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Nabumetone is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 72189-0184-90
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nabumetone

Product Information

NDC	72189-0184
Product ID	72189-184_ff32e332-8830-e529-e053-6394a90acd5d
Associated GPIs	66100055000320
GCN Sequence Number	016574
GCN Sequence Number Description	nabumetone TABLET 500 MG ORAL
HIC3	S2B
HIC3 Description	NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
GCN	32961
HICL Sequence Number	006311
HICL Sequence Number Description	NABUMETONE
Brand/Generic	Generic
Proprietary Name	NABUMETONE
Proprietary Name Suffix	n/a
Non-Proprietary Name	NABUMETONE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	NABUMETONE
Labeler Name	direct rx
Pharmaceutical Class	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078420
Listing Certified Through	2024-12-31

Package

NDC 72189-0184-90 (72189018490)

Pricing Information	N/A
NDC Package Code	72189-184-90
Billing NDC	72189018490
Package	90 TABLET in 1 BOTTLE (72189-184-90)
Marketing Start Date	2021-05-11
NDC Exclude Flag	N