CAMBIA - 50192-113-09 - (Diclofenac Potassium)

Alphabetical Index


Drug Information of CAMBIA

Product NDC: 50192-113
Proprietary Name: CAMBIA
Non Proprietary Name: Diclofenac Potassium
Active Ingredient(s): 1    mg/mg & nbsp;   Diclofenac Potassium
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CAMBIA

Product NDC: 50192-113
Labeler Name: Nautilus Neurosciences, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022165
Marketing Category: NDA
Start Marketing Date: 20100420

Package Information of CAMBIA

Package NDC: 50192-113-09
Package Description: 9 PACKET in 1 BOX (50192-113-09) > 50 mg in 1 PACKET

NDC Information of CAMBIA

NDC Code 50192-113-09
Proprietary Name CAMBIA
Package Description 9 PACKET in 1 BOX (50192-113-09) > 50 mg in 1 PACKET
Product NDC 50192-113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Potassium
Dosage Form Name POWDER, FOR SOLUTION
Route Name ORAL
Start Marketing Date 20100420
Marketing Category Name NDA
Labeler Name Nautilus Neurosciences, Inc.
Substance Name DICLOFENAC POTASSIUM
Strength Number 1
Strength Unit mg/mg
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of CAMBIA


General Information