Search by Drug Name or NDC

NDC 68788-7341-01 Flurbiprofen 100 mg/1 Details

Flurbiprofen 100 mg/1

Flurbiprofen is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is FLURBIPROFEN.

MedlinePlus Drug Summary

Flurbiprofen 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). Flurbiprofen 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: 68788-7341-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Flurbiprofen

Product Information

NDC	68788-7341
Product ID	68788-7341_71057574-1b88-42a6-a5bd-c2144044726a
Associated GPIs	66100012000315
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	Flurbiprofen
Proprietary Name Suffix	n/a
Non-Proprietary Name	Flurbiprofen
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	FLURBIPROFEN
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	ANDA074431
Listing Certified Through	2024-12-31

Package

NDC 68788-7341-01 (68788734101)

Pricing Information	N/A
NDC Package Code	68788-7341-1
Billing NDC	68788734101
Package	100 TABLET, FILM COATED in 1 BOTTLE (68788-7341-1)
Marketing Start Date	2019-03-08
NDC Exclude Flag	N