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Diclofenac Potassium - 0781-5017-10 - (Diclofenac Potassium)

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Drug Information of Diclofenac Potassium

Product NDC: 0781-5017
Proprietary Name: Diclofenac Potassium
Non Proprietary Name: Diclofenac Potassium
Active Ingredient(s): 50    mg/1 & nbsp;   Diclofenac Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Potassium

Product NDC: 0781-5017
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075229
Marketing Category: ANDA
Start Marketing Date: 19981120

Package Information of Diclofenac Potassium

Package NDC: 0781-5017-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5017-10)

NDC Information of Diclofenac Potassium

NDC Code 0781-5017-10
Proprietary Name Diclofenac Potassium
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5017-10)
Product NDC 0781-5017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19981120
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DICLOFENAC POTASSIUM
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Diclofenac Potassium


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