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Sandostatin - octreotide acetate

Navigation: NDC > Supplier starting with: N > NOVARTIS PHARMACEUTICALS CORPORATION
Field Value
NDC Code: 0078-0184
Proprietary Name: Sandostatin
Suffix:
Non-Proprietary Name: octreotide acetate
Dosage Form: INJECTION, SOLUTION
Method: INTRAVENOUS; SUBCUTANEOUS
Original Marketing Date: 21-10-1988
Category Name: NDA
Application Number: NDA019667
Labeler: NOVARTIS PHARMACEUTICALS CORPORATION
Substance Name: OCTREOTIDE ACETATE
Active Numerator Strength: 1000
Active Ingredient Unit: ug/mL
Pharm Classes: Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]
DEA Schedule: