Zipsor - 35356-537-60 - (diclofenac potassium)

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Drug Information of Zipsor

Product NDC: 35356-537
Proprietary Name: Zipsor
Non Proprietary Name: diclofenac potassium
Active Ingredient(s): 25    mg/1 & nbsp;   diclofenac potassium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Zipsor

Product NDC: 35356-537
Labeler Name: Lake Erie Medical DBA Quality Care Products
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022202
Marketing Category: NDA
Start Marketing Date: 20101222

Package Information of Zipsor

Package NDC: 35356-537-60
Package Description: 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (35356-537-60)

NDC Information of Zipsor

NDC Code 35356-537-60
Proprietary Name Zipsor
Package Description 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (35356-537-60)
Product NDC 35356-537
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diclofenac potassium
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20101222
Marketing Category Name NDA
Labeler Name Lake Erie Medical DBA Quality Care Products
Substance Name DICLOFENAC POTASSIUM
Strength Number 25
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 Zipsor


General Information