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Diclofenac Sodium - 63629-3941-2 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 63629-3941
Proprietary Name: Diclofenac Sodium
Non Proprietary Name: Diclofenac Sodium
Active Ingredient(s): 100    mg/1 & nbsp;   Diclofenac Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Sodium

Product NDC: 63629-3941
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075910
Marketing Category: ANDA
Start Marketing Date: 20040302

Package Information of Diclofenac Sodium

Package NDC: 63629-3941-2
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3941-2)

NDC Information of Diclofenac Sodium

NDC Code 63629-3941-2
Proprietary Name Diclofenac Sodium
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3941-2)
Product NDC 63629-3941
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040302
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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 Diclofenac Sodium


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