FDA NDC Directory · JSON-LD · Markdown

HUMATROPE

NDC 0002-8147 · HUMAN PRESCRIPTION DRUG · KIT

Generic nameSomatropin
Labeler / ManufacturerEli Lilly and Company
Marketing categoryBiologic License Application · App BLA019640
Dosage form / routeKIT · INTRAMUSCULAR SUBCUTANEOUS
Active ingredients—
Marketing started20060127
Package count1

External sources

Source: openFDA. Public-domain (CC0).