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Diclofenac Sodium Delayed Release - 52125-297-02 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium Delayed Release

Product NDC: 52125-297
Proprietary Name: Diclofenac Sodium Delayed Release
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 Delayed Release

Product NDC: 52125-297
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075185
Marketing Category: ANDA
Start Marketing Date: 20130604

Package Information of Diclofenac Sodium Delayed Release

Package NDC: 52125-297-02
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (52125-297-02)

NDC Information of Diclofenac Sodium Delayed Release

NDC Code 52125-297-02
Proprietary Name Diclofenac Sodium Delayed Release
Package Description 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (52125-297-02)
Product NDC 52125-297
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130604
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 Delayed Release


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