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"0781-1789-10" National Drug Code (NDC)
Diclofenac Sodium 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1789-10)
(Sandoz Inc)
NDC Code
0781-1789-10
Package Description
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1789-10)
Product NDC
0781-1789
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium
Non-Proprietary Name
Diclofenac Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
19951130
End Marketing Date
20190831
Marketing Category Name
ANDA
Application Number
ANDA074394
Manufacturer
Sandoz Inc
Substance Name
DICLOFENAC SODIUM
Strength
75
Strength Unit
mg/1
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/0781-1789-10