Voltaren - 0078-0446-05 - (diclofenac sodium extended release tablets)

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Drug Information of Voltaren

Product NDC: 0078-0446
Proprietary Name: Voltaren
Non Proprietary Name: diclofenac sodium extended release tablets
Active Ingredient(s): 100    mg/1 & nbsp;   diclofenac sodium extended release tablets
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Voltaren

Product NDC: 0078-0446
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020254
Marketing Category: NDA
Start Marketing Date: 19960308

Package Information of Voltaren

Package NDC: 0078-0446-05
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0078-0446-05)

NDC Information of Voltaren

NDC Code 0078-0446-05
Proprietary Name Voltaren
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0078-0446-05)
Product NDC 0078-0446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac sodium extended release tablets
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19960308
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name DICLOFENAC SODIUM
Strength Number 100
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 Voltaren


General Information