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"0078-0182-01" National Drug Code (NDC)
Sandostatin 10 AMPULE in 1 PACKAGE (0078-0182-01) / 1 mL in 1 AMPULE (0078-0182-61)
(Novartis Pharmaceuticals Corporation)
NDC Code
0078-0182-01
Package Description
10 AMPULE in 1 PACKAGE (0078-0182-01) / 1 mL in 1 AMPULE (0078-0182-61)
Product NDC
0078-0182
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sandostatin
Non-Proprietary Name
Octreotide Acetate
Dosage Form
INJECTION, SOLUTION
Usage
INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date
19881021
Marketing Category Name
NDA
Application Number
NDA019667
Manufacturer
Novartis Pharmaceuticals Corporation
Substance Name
OCTREOTIDE ACETATE
Strength
500
Strength Unit
ug/mL
Pharmacy Classes
Somatostatin Analog [EPC], Somatostatin Receptor Agonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0078-0182-01