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NDC 68788-7765-02 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 Preferred Pharmaceuticals, Inc.. 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: 68788-7765-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nabumetone

Product Information

NDC	68788-7765
Product ID	68788-7765_ca79a1a0-f306-4f52-aa81-e571949441b0
Associated GPIs	66100055000320
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
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	NABUMETONE
Labeler Name	Preferred Pharmaceuticals, Inc.
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 68788-7765-02 (68788776502)

Pricing Information	N/A
NDC Package Code	68788-7765-2
Billing NDC	68788776502
Package	20 TABLET in 1 BOTTLE (68788-7765-2)
Marketing Start Date	2020-07-15
NDC Exclude Flag	N