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Diclofenac Sodium - 68387-260-60 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 68387-260
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: 68387-260
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077863
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Diclofenac Sodium

Package NDC: 68387-260-60
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68387-260-60)

NDC Information of Diclofenac Sodium

NDC Code 68387-260-60
Proprietary Name Diclofenac Sodium
Package Description 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68387-260-60)
Product NDC 68387-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals 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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