Octreotide Acetate (Sandoz Inc)
Welcome to the PulseAid listing for the Octreotide Acetate drug offered from Sandoz Inc. This Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Sandoz Inc |
NON-PROPRIETARY NAME: | Octreotide Acetate |
SUBSTANCE NAME: | OCTREOTIDE ACETATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA] |
ROUTE: | INTRAVENOUS; SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1988-10-21 |
END MARKETING DATE: | 0000-00-00 |
Octreotide Acetate HUMAN PRESCRIPTION DRUG Details:
Item Description | Octreotide Acetate from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1000(ug/mL) |
START MARKETING DATE: | 1988-10-21 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-3164_b02b276f-9007-4ec7-8bcd-40f14213d7f5 |
PRODUCT NDC: | 0781-3164 |
APPLICATION NUMBER: | NDA019667 |
Other OCTREOTIDE ACETATE Pharmaceutical Manufacturers / Labelers: