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Diclofenac Sodium - 0591-0338-10 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 0591-0338
Proprietary Name: Diclofenac Sodium
Non Proprietary Name: Diclofenac Sodium
Active Ingredient(s): 50    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: 0591-0338
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075185
Marketing Category: ANDA
Start Marketing Date: 19981113

Package Information of Diclofenac Sodium

Package NDC: 0591-0338-10
Package Description: 12 BOTTLE, PLASTIC in 1 BOX (0591-0338-10) > 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

NDC Information of Diclofenac Sodium

NDC Code 0591-0338-10
Proprietary Name Diclofenac Sodium
Package Description 12 BOTTLE, PLASTIC in 1 BOX (0591-0338-10) > 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC 0591-0338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19981113
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name DICLOFENAC SODIUM
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 Sodium


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