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Diclofenac Sodium - 0781-1789-10 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 0781-1789
Proprietary Name: Diclofenac Sodium
Non Proprietary Name: Diclofenac Sodium
Active Ingredient(s): 75    mg/1 & nbsp;   Diclofenac Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Sodium

Product NDC: 0781-1789
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074394
Marketing Category: ANDA
Start Marketing Date: 19951130

Package Information of Diclofenac Sodium

Package NDC: 0781-1789-10
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1789-10)

NDC Information of Diclofenac Sodium

NDC Code 0781-1789-10
Proprietary Name Diclofenac Sodium
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1789-10)
Product NDC 0781-1789
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19951130
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DICLOFENAC SODIUM
Strength Number 75
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 Sodium


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