Package 25021-463-01
Brand: octreotide acetate
Generic: octreotide acetatePackage Facts
Identity
Package NDC
25021-463-01
Digits Only
2502146301
Product NDC
25021-463
Description
10 VIAL in 1 CARTON (25021-463-01) / 1 mL in 1 VIAL
Marketing
Marketing Status
Brand
octreotide acetate
Generic
octreotide acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "5e508c59-4170-441a-a94a-70b0bf28b8e4", "openfda": {"unii": ["75R0U2568I"], "rxcui": ["312068", "312069", "312070", "312071", "314152"], "spl_set_id": ["7ce2fc1e-7520-4d04-be45-2baba32ca24a"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-463-01) / 1 mL in 1 VIAL", "package_ndc": "25021-463-01", "marketing_start_date": "20230615"}], "brand_name": "Octreotide Acetate", "product_id": "25021-463_5e508c59-4170-441a-a94a-70b0bf28b8e4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "25021-463", "generic_name": "octreotide acetate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Octreotide Acetate", "active_ingredients": [{"name": "OCTREOTIDE ACETATE", "strength": "50 ug/mL"}], "application_number": "ANDA090834", "marketing_category": "ANDA", "marketing_start_date": "20230615", "listing_expiration_date": "20261231"}