Home NDC 0002-7555 NDC 0002-7555 - HUMATROPE This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 0002-7555
Package NDCs from labels 0002-7555-01
Manufacturer Eli Lilly and Company
Effective date 2025-11-25
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type HUMATROPE - Eli Lilly and Company Eli Lilly and Company 2025-11-25 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0002-7555-01 HUMATROPE 2.88 mL in 1 CARTRIDGE INJECTION, POWDER, FOR SOLUTION 2.88 mL 12 mg in 2.88mL 44
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0002-7555 HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY] 41 Unmatched 20241212_a774e1ae-3997-49ee-8b0e-99a2b315d409.zip
DailyMed Socrata Ingredients#