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FLURBIPROFEN - 16590-096-30 - (FLURBIPROFEN)

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Drug Information of FLURBIPROFEN

Product NDC: 16590-096
Proprietary Name: FLURBIPROFEN
Non Proprietary Name: FLURBIPROFEN
Active Ingredient(s): 100    mg/1 & nbsp;   FLURBIPROFEN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of FLURBIPROFEN

Product NDC: 16590-096
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074358
Marketing Category: ANDA
Start Marketing Date: 19940620

Package Information of FLURBIPROFEN

Package NDC: 16590-096-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-096-30)

NDC Information of FLURBIPROFEN

NDC Code 16590-096-30
Proprietary Name FLURBIPROFEN
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-096-30)
Product NDC 16590-096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLURBIPROFEN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940620
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name FLURBIPROFEN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of FLURBIPROFEN


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