Package 0002-8501-01
Brand: humulin r u-500
Generic: insulin humanPackage Facts
Identity
Package NDC
0002-8501-01
Digits Only
0002850101
Product NDC
0002-8501
Description
1 VIAL, MULTI-DOSE in 1 CARTON (0002-8501-01) / 20 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
Brand
humulin r u-500
Generic
insulin human
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "7872727a-5d70-410a-ad64-b3b47afceb5e", "openfda": {"nui": ["M0011417", "N0000175944"], "unii": ["1Y17CTI5SR"], "rxcui": ["249220", "351859", "1731315", "1731317"], "spl_set_id": ["b60e8dd0-1d48-4dc9-87fd-e14675255e8c"], "pharm_class_cs": ["Insulin [CS]"], "pharm_class_epc": ["Insulin [EPC]"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0002-8501-01) / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0002-8501-01", "marketing_start_date": "19970106"}], "brand_name": "Humulin R U-500", "product_id": "0002-8501_7872727a-5d70-410a-ad64-b3b47afceb5e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Insulin [CS]", "Insulin [EPC]"], "product_ndc": "0002-8501", "generic_name": "Insulin human", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Humulin", "brand_name_suffix": "R U-500", "active_ingredients": [{"name": "INSULIN HUMAN", "strength": "500 [iU]/mL"}], "application_number": "BLA018780", "marketing_category": "BLA", "marketing_start_date": "19940331", "listing_expiration_date": "20261231"}