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Diclofenac Potassium - 21695-838-42 - (Diclofenac Potassium)

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Drug Information of Diclofenac Potassium

Product NDC: 21695-838
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: 21695-838
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075219
Marketing Category: ANDA
Start Marketing Date: 20100121

Package Information of Diclofenac Potassium

Package NDC: 21695-838-42
Package Description: 42 TABLET, FILM COATED in 1 BOTTLE (21695-838-42)

NDC Information of Diclofenac Potassium

NDC Code 21695-838-42
Proprietary Name Diclofenac Potassium
Package Description 42 TABLET, FILM COATED in 1 BOTTLE (21695-838-42)
Product NDC 21695-838
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100121
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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