ARTHROTEC - 63629-3359-2 - (diclofenac sodium and misoprostol)

Alphabetical Index


Drug Information of ARTHROTEC

Product NDC: 63629-3359
Proprietary Name: ARTHROTEC
Non Proprietary Name: diclofenac sodium and misoprostol
Active Ingredient(s): 75; 200    mg/1; ug/1 & nbsp;   diclofenac sodium and misoprostol
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ARTHROTEC

Product NDC: 63629-3359
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020607
Marketing Category: NDA
Start Marketing Date: 19971224

Package Information of ARTHROTEC

Package NDC: 63629-3359-2
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (63629-3359-2)

NDC Information of ARTHROTEC

NDC Code 63629-3359-2
Proprietary Name ARTHROTEC
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (63629-3359-2)
Product NDC 63629-3359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac sodium and misoprostol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19971224
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name DICLOFENAC SODIUM; MISOPROSTOL
Strength Number 75; 200
Strength Unit mg/1; ug/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient]

Complete Information of ARTHROTEC


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