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Diclofenac Sodium Extended-Release - 21695-040-30 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium Extended-Release

Product NDC: 21695-040
Proprietary Name: Diclofenac Sodium Extended-Release
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 Extended-Release

Product NDC: 21695-040
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075910
Marketing Category: ANDA
Start Marketing Date: 20020107

Package Information of Diclofenac Sodium Extended-Release

Package NDC: 21695-040-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-040-30)

NDC Information of Diclofenac Sodium Extended-Release

NDC Code 21695-040-30
Proprietary Name Diclofenac Sodium Extended-Release
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-040-30)
Product NDC 21695-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020107
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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 Extended-Release


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