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NDC 51655-0396-25 Nabumetone 500 mg/1 Details

Nabumetone 500 mg/1

Nabumetone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. 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: 51655-0396-25
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Nabumetone

Product Information

NDC	51655-0396
Product ID	51655-396_08a49589-0c4f-2988-e063-6394a90a6fcb
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Nabumetone
Proprietary Name Suffix	n/a
Non-Proprietary Name	Nabumetone
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	NABUMETONE
Labeler Name	Northwind Pharmaceuticals, LLC
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	ANDA078671
Listing Certified Through	2024-12-31

Package

NDC 51655-0396-25 (51655039625)

Pricing Information	N/A
NDC Package Code	51655-396-25
Billing NDC	51655039625
Package	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-396-25)
Marketing Start Date	2020-07-07
NDC Exclude Flag	N