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NDC 70934-0013-20 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. 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: 70934-0013-20
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nabumetone

Product Information

NDC	70934-0013
Product ID	70934-013_d672b3a2-c559-5111-e053-2995a90a0cb3
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	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
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	2023-12-31

Package

NDC 70934-0013-20 (70934001320)

Pricing Information	N/A
NDC Package Code	70934-013-20
Billing NDC	70934001320
Package	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-013-20)
Marketing Start Date	2019-02-05
NDC Exclude Flag	N