Package 0002-0800-01
Brand: sterile diluent
Generic: diluentPackage Facts
Identity
Package NDC
0002-0800-01
Digits Only
0002080001
Product NDC
0002-0800
Description
1 VIAL in 1 CARTON (0002-0800-01) / 10 mL in 1 VIAL
Marketing
Marketing Status
Brand
sterile diluent
Generic
diluent
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "3d52c48f-89cd-4d3d-8db6-1789e76a1c79", "openfda": {"nui": ["N0000004931", "N0000175453"], "unii": ["059QF0KO0R", "GFX7QIS1II"], "rxcui": ["242120", "865098", "1652239", "1652242", "1652639", "1652640", "1652644", "1652646", "1926331", "1926332", "2621571", "2621572"], "spl_set_id": ["c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f"], "pharm_class_cs": ["Insulin [Chemical/Ingredient]"], "pharm_class_epc": ["Insulin Analog [EPC]"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0002-0800-01) / 10 mL in 1 VIAL", "package_ndc": "0002-0800-01", "marketing_start_date": "19870710"}], "brand_name": "Sterile Diluent", "product_id": "0002-0800_3d52c48f-89cd-4d3d-8db6-1789e76a1c79", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0002-0800", "generic_name": "diluent", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sterile Diluent", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "BLA020563", "marketing_category": "BLA", "marketing_start_date": "19870710", "listing_expiration_date": "20261231"}