sandostatin

Generic: octreotide acetate

Labeler: novartis pharmaceuticals corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sandostatin
Generic Name octreotide acetate
Labeler novartis pharmaceuticals corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

octreotide acetate 100 ug/mL

Manufacturer
Novartis Pharmaceuticals Corporation

Identifiers & Regulatory

Product NDC 0078-0181
Product ID 0078-0181_ad42b59d-8ad5-4855-96a9-f40c7ef4a7e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019667
Listing Expiration 2026-12-31
Marketing Start 1988-10-21

Pharmacologic Class

Classes
somatostatin analog [epc] somatostatin receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00780181
Hyphenated Format 0078-0181

Supplemental Identifiers

RxCUI
207194 207198 207200 312068 312069 312070
UNII
75R0U2568I

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sandostatin (source: ndc)
Generic Name octreotide acetate (source: ndc)
Application Number NDA019667 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 100 ug/mL
source: ndc
Packaging
  • 10 AMPULE in 1 PACKAGE (0078-0181-01) / 1 mL in 1 AMPULE (0078-0181-61)
source: ndc

Packages (1)

0078-0181-01 10 AMPULE in 1 PACKAGE (0078-0181-01) / 1 mL in 1 AMPULE (0078-0181-61)

Ingredients (1)

octreotide acetate (100 ug/mL)

Linked Drug Pages (1)

Sandostatin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "ad42b59d-8ad5-4855-96a9-f40c7ef4a7e3", "openfda": {"unii": ["75R0U2568I"], "rxcui": ["207194", "207198", "207200", "312068", "312069", "312070"], "spl_set_id": ["4e2c9856-1836-49f0-9472-4dbeeb408f39"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 PACKAGE (0078-0181-01)  / 1 mL in 1 AMPULE (0078-0181-61)", "package_ndc": "0078-0181-01", "marketing_start_date": "19881021"}], "brand_name": "Sandostatin", "product_id": "0078-0181_ad42b59d-8ad5-4855-96a9-f40c7ef4a7e3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "0078-0181", "generic_name": "octreotide acetate", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sandostatin", "active_ingredients": [{"name": "OCTREOTIDE ACETATE", "strength": "100 ug/mL"}], "application_number": "NDA019667", "marketing_category": "NDA", "marketing_start_date": "19881021", "listing_expiration_date": "20261231"}