NDC 0002-7554-01 - 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: 0002-7554
Requested NDC: 0002-7554-01
Package NDCs from labels: 0002-7554-01
Manufacturer: Eli Lilly and Company
Effective date: 2026-08-20
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	2026-08-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0002-7554-01	HUMATROPE	2.88 mL in 1 CARTRIDGE	INJECTION, POWDER, FOR SOLUTION	2.88 mL	6 mg in 2.88mL	44

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0002-7554	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	41	Unmatched	20241212_a774e1ae-3997-49ee-8b0e-99a2b315d409.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Somatropin	ACTIVE INGREDIENT	NQX9KB6PCL	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
Somatropin	ACTIVE MOIETY	NQX9KB6PCL	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
glycine	INACTIVE INGREDIENT	TE7660XO1C	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
mannitol	INACTIVE INGREDIENT	3OWL53L36A	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
phosphoric acid	INACTIVE INGREDIENT	E4GA8884NN	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
sodium hydroxide	INACTIVE INGREDIENT	55X04QC32I	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24
sodium phosphate, dibasic	INACTIVE INGREDIENT	GR686LBA74	HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]	24

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 46 of 46 · 902 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21		Exact identifier unii: 70WT22SF4B

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.