Package 0002-8805-59

Brand: humulin n

Generic: insulin human
NDC Package

Package Facts

Identity

Package NDC 0002-8805-59
Digits Only 0002880559
Product NDC 0002-8805
Description

5 SYRINGE in 1 CARTON (0002-8805-59) / 3 mL in 1 SYRINGE (0002-8805-01)

Marketing

Marketing Status
Marketed Since 2014-01-17
Brand humulin n
Generic insulin human
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "79bc67f8-8bf8-4e92-bdd9-3e0700e6d9db", "openfda": {"nui": ["M0011417", "N0000175944"], "upc": ["0300028315019"], "unii": ["1Y17CTI5SR"], "rxcui": ["311026", "311028", "847199", "1654862"], "spl_set_id": ["f6edd793-440b-40c2-96b5-c16133b7a921"], "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": "5 SYRINGE in 1 CARTON (0002-8805-59)  / 3 mL in 1 SYRINGE (0002-8805-01)", "package_ndc": "0002-8805-59", "marketing_start_date": "20140117"}], "brand_name": "Humulin N", "product_id": "0002-8805_79bc67f8-8bf8-4e92-bdd9-3e0700e6d9db", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Insulin [CS]", "Insulin [EPC]"], "product_ndc": "0002-8805", "generic_name": "Insulin human", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Humulin", "brand_name_suffix": "N", "active_ingredients": [{"name": "INSULIN HUMAN", "strength": "100 [iU]/mL"}], "application_number": "BLA018781", "marketing_category": "BLA", "marketing_start_date": "20131107", "listing_expiration_date": "20261231"}