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Diclofenac Potassium - 49999-593-20 - (diclofenac potassium)

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Drug Information of Diclofenac Potassium

Product NDC: 49999-593
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Potassium

Product NDC: 49999-593
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075463
Marketing Category: ANDA
Start Marketing Date: 20111205

Package Information of Diclofenac Potassium

Package NDC: 49999-593-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (49999-593-20)

NDC Information of Diclofenac Potassium

NDC Code 49999-593-20
Proprietary Name Diclofenac Potassium
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (49999-593-20)
Product NDC 49999-593
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111205
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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