Package 0078-0180-01

Brand: sandostatin

Generic: octreotide acetate
NDC Package

Package Facts

Identity

Package NDC 0078-0180-01
Digits Only 0078018001
Product NDC 0078-0180
Product ID 0078-0180_ad42b59d-8ad5-4855-96a9-f40c7ef4a7e3
Description

10 AMPULE in 1 PACKAGE (0078-0180-01) / 1 mL in 1 AMPULE (0078-0180-61)

Marketing

Marketing Status
Marketed Since 1988-10-21
Brand sandostatin
Generic octreotide acetate
Sample Package No

Linked Drug Pages (1)

Sandostatin ndc-match (0.95)

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 (0078-0180-01)  / 1 mL in 1 AMPULE (0078-0180-61)", "package_ndc": "0078-0180-01", "marketing_start_date": "19881021"}], "brand_name": "Sandostatin", "product_id": "0078-0180_ad42b59d-8ad5-4855-96a9-f40c7ef4a7e3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "0078-0180", "generic_name": "octreotide acetate", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sandostatin", "active_ingredients": [{"name": "OCTREOTIDE ACETATE", "strength": "50 ug/mL"}], "application_number": "NDA019667", "marketing_category": "NDA", "marketing_start_date": "19881021", "listing_expiration_date": "20261231"}