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NDC 63629-8338-01 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 Bryant Ranch Prepack. 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: 63629-8338-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Flurbiprofen

Product Information

NDC	63629-8338
Product ID	63629-8338_b018b566-3288-430e-b430-2a2d37f8da9d
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	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	Bryant Ranch Prepack
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 63629-8338-01 (63629833801)

Pricing Information	N/A
NDC Package Code	63629-8338-1
Billing NDC	63629833801
Package	30 TABLET, FILM COATED in 1 BOTTLE (63629-8338-1)
Marketing Start Date	2021-12-23
NDC Exclude Flag	N