humatrope
Generic: somatropin
Labeler: eli lilly and companyDrug Facts
Product Profile
Brand Name
humatrope
Generic Name
somatropin
Labeler
eli lilly and company
Dosage Form
KIT
Routes
Manufacturer
Identifiers & Regulatory
Product NDC
0002-8147
Product ID
0002-8147_65052345-9f7f-4580-8cff-1e61a421843c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA019640
Listing Expiration
2026-12-31
Marketing Start
2006-01-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00028147
Hyphenated Format
0002-8147
Supplemental Identifiers
RxCUI
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
humatrope (source: ndc)
Generic Name
somatropin (source: ndc)
Application Number
BLA019640 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 mg
- 12 mg
- 24 mg
Packaging
- 1 TRAY in 1 CARTON (0002-8147-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "SUBCUTANEOUS"], "spl_id": "65052345-9f7f-4580-8cff-1e61a421843c", "openfda": {"rxcui": ["582969", "582971", "582974", "582976", "729232", "729234"], "spl_set_id": ["a774e1ae-3997-49ee-8b0e-99a2b315d409"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TRAY in 1 CARTON (0002-8147-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)", "package_ndc": "0002-8147-01", "marketing_start_date": "20060127"}], "brand_name": "HUMATROPE", "product_id": "0002-8147_65052345-9f7f-4580-8cff-1e61a421843c", "dosage_form": "KIT", "product_ndc": "0002-8147", "generic_name": "Somatropin", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HUMATROPE", "application_number": "BLA019640", "marketing_category": "BLA", "marketing_start_date": "20060127", "listing_expiration_date": "20261231"}