humulin n
Generic: insulin human
Labeler: eli lilly and companyDrug Facts
Product Profile
Brand Name
humulin n
Generic Name
insulin human
Labeler
eli lilly and company
Dosage Form
INJECTION, SUSPENSION
Routes
Active Ingredients
insulin human 100 [iU]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0002-8805
Product ID
0002-8805_79bc67f8-8bf8-4e92-bdd9-3e0700e6d9db
Product Type
HUMAN OTC DRUG
Marketing Category
BLA
Application Number
BLA018781
Listing Expiration
2026-12-31
Marketing Start
2013-11-07
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00028805
Hyphenated Format
0002-8805
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
humulin n (source: ndc)
Generic Name
insulin human (source: ndc)
Application Number
BLA018781 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 [iU]/mL
Packaging
- 5 SYRINGE in 1 CARTON (0002-8805-59) / 3 mL in 1 SYRINGE (0002-8805-01)
Packages (1)
Ingredients (1)
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"}