humatrope

Generic: somatropin

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name humatrope
Generic Name somatropin
Labeler eli lilly and company
Dosage Form KIT
Routes
INTRAMUSCULAR SUBCUTANEOUS
Manufacturer
Eli Lilly and Company

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
582969 582971 582974 582976 729232 729234

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg
  • 12 mg
  • 24 mg
source: label
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)
source: ndc

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"}