Package 0002-7737-01
Brand: insulin lispro
Generic: insulin lisproPackage Facts
Identity
Package NDC
0002-7737-01
Digits Only
0002773701
Product NDC
0002-7737
Description
1 VIAL in 1 CARTON (0002-7737-01) / 10 mL in 1 VIAL
Marketing
Marketing Status
Brand
insulin lispro
Generic
insulin lispro
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6329aa6b-3571-4196-83b0-fc99de56f3ab", "openfda": {"nui": ["N0000004931", "N0000175453"], "unii": ["GFX7QIS1II"], "rxcui": ["242120", "1652639", "1926331"], "spl_set_id": ["97d5e596-aae1-42c9-ae89-c3780959c467"], "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 (0002-7737-01) / 10 mL in 1 VIAL", "package_ndc": "0002-7737-01", "marketing_start_date": "20200212"}], "brand_name": "Insulin Lispro", "product_id": "0002-7737_6329aa6b-3571-4196-83b0-fc99de56f3ab", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Insulin Analog [EPC]", "Insulin [Chemical/Ingredient]"], "product_ndc": "0002-7737", "generic_name": "Insulin lispro", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Insulin Lispro", "active_ingredients": [{"name": "INSULIN LISPRO", "strength": "100 [iU]/mL"}], "application_number": "BLA020563", "marketing_category": "BLA", "marketing_start_date": "20200212", "listing_expiration_date": "20261231"}