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"50192-113-01" National Drug Code (NDC)
Cambia 50 mg in 1 PACKET (50192-113-01)
(Nautilus Neurosciences, Inc.)
NDC Code
50192-113-01
Package Description
50 mg in 1 PACKET (50192-113-01)
Product NDC
50192-113
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cambia
Non-Proprietary Name
Diclofenac Potassium
Dosage Form
POWDER, FOR SOLUTION
Usage
ORAL
Start Marketing Date
20100420
Marketing Category Name
NDA
Application Number
NDA022165
Manufacturer
Nautilus Neurosciences, Inc.
Substance Name
DICLOFENAC POTASSIUM
Strength
1
Strength Unit
mg/mg
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50192-113-01