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"0078-0183-25" National Drug Code (NDC)

Sandostatin 1 VIAL, MULTI-DOSE in 1 BOX (0078-0183-25) > 5 mL in 1 VIAL, MULTI-DOSE
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0183-25
Package Description1 VIAL, MULTI-DOSE in 1 BOX (0078-0183-25) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC0078-0183
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSandostatin
Non-Proprietary NameOctreotide Acetate
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS; SUBCUTANEOUS
Start Marketing Date19881021
End Marketing Date20190731
Marketing Category NameNDA
Application NumberNDA019667
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameOCTREOTIDE ACETATE
Strength200
Strength Unitug/mL
Pharmacy ClassesSomatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

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