"0078-0181-01" National Drug Code (NDC)

Sandostatin 10 AMPULE in 1 PACKAGE (0078-0181-01) / 1 mL in 1 AMPULE (0078-0181-61)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0181-01
Package Description10 AMPULE in 1 PACKAGE (0078-0181-01) / 1 mL in 1 AMPULE (0078-0181-61)
Product NDC0078-0181
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSandostatin
Non-Proprietary NameOctreotide Acetate
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS; SUBCUTANEOUS
Start Marketing Date19881021
Marketing Category NameNDA
Application NumberNDA019667
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameOCTREOTIDE ACETATE
Strength100
Strength Unitug/mL
Pharmacy ClassesSomatostatin Analog [EPC], Somatostatin Receptor Agonists [MoA]

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