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Diclofenac Potassium - 49349-955-04 - (Diclofenac Potassium)

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Drug Information of Diclofenac Potassium

Product NDC: 49349-955
Proprietary Name: Diclofenac Potassium
Non Proprietary Name: Diclofenac Potassium
Active Ingredient(s): 50    mg/1 & nbsp;   Diclofenac Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Potassium

Product NDC: 49349-955
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075219
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Diclofenac Potassium

Package NDC: 49349-955-04
Package Description: 14 TABLET in 1 BLISTER PACK (49349-955-04)

NDC Information of Diclofenac Potassium

NDC Code 49349-955-04
Proprietary Name Diclofenac Potassium
Package Description 14 TABLET in 1 BLISTER PACK (49349-955-04)
Product NDC 49349-955
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Potassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DICLOFENAC POTASSIUM
Strength Number 50
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 Potassium


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