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Diclofenac Sodium - 68788-9787-8 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 68788-9787
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: 68788-9787
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075910
Marketing Category: ANDA
Start Marketing Date: 20120604

Package Information of Diclofenac Sodium

Package NDC: 68788-9787-8
Package Description: 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9787-8)

NDC Information of Diclofenac Sodium

NDC Code 68788-9787-8
Proprietary Name Diclofenac Sodium
Package Description 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9787-8)
Product NDC 68788-9787
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120604
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
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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