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NDC 43063-0992-15 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 PD-Rx 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: 43063-0992-15
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Flurbiprofen

Product Information

NDC	43063-0992
Product ID	43063-992_f8395a5c-e5a3-3d70-e053-6394a90a02b5
Associated GPIs	66100012000315
GCN Sequence Number	008363
GCN Sequence Number Description	flurbiprofen TABLET 100 MG ORAL
HIC3	S2B
HIC3 Description	NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
GCN	35711
HICL Sequence Number	003728
HICL Sequence Number Description	FLURBIPROFEN
Brand/Generic	Generic
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	PD-Rx 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 43063-0992-15 (43063099215)

Pricing Information	N/A
NDC Package Code	43063-992-15
Billing NDC	43063099215
Package	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-992-15)
Marketing Start Date	2016-06-18
NDC Exclude Flag	N