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Diclofenac Sodium - 49349-276-02 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 49349-276
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: 49349-276
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074394
Marketing Category: ANDA
Start Marketing Date: 20110602

Package Information of Diclofenac Sodium

Package NDC: 49349-276-02
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-276-02)

NDC Information of Diclofenac Sodium

NDC Code 49349-276-02
Proprietary Name Diclofenac Sodium
Package Description 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-276-02)
Product NDC 49349-276
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110602
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


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