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NDC 71205-0030-20 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 Proficient Rx LP. 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: 71205-0030-20
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nabumetone

Product Information

NDC	71205-0030
Product ID	71205-030_55d8ea63-038a-4294-9243-ca915460c1a6
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, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	NABUMETONE
Labeler Name	Proficient Rx LP
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	ANDA091083
Listing Certified Through	2024-12-31

Package

NDC 71205-0030-20 (71205003020)

Pricing Information	N/A
NDC Package Code	71205-030-20
Billing NDC	71205003020
Package	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-20)
Marketing Start Date	2022-01-19
NDC Exclude Flag	N