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DICLOFENAC SODIUM - 35356-776-60 - (diclofenac sodium)

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Drug Information of DICLOFENAC SODIUM

Product NDC: 35356-776
Proprietary Name: DICLOFENAC SODIUM
Non Proprietary Name: diclofenac sodium
Active Ingredient(s): 100    mg/1 & nbsp;   diclofenac sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of DICLOFENAC SODIUM

Product NDC: 35356-776
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075910
Marketing Category: ANDA
Start Marketing Date: 20020109

Package Information of DICLOFENAC SODIUM

Package NDC: 35356-776-60
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (35356-776-60)

NDC Information of DICLOFENAC SODIUM

NDC Code 35356-776-60
Proprietary Name DICLOFENAC SODIUM
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (35356-776-60)
Product NDC 35356-776
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac sodium
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020109
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name DICLOFENAC SODIUM
Strength Number 100
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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