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This release contains forward-looking information about NGENLA (somatrogon-ghla) Safety Information Somatropin should not be used in children and adults receiving somatropin treatment, treatment should be monitored carefully for any malignant transformation of skin lesions. NASDAQ: OPK) announced today that the U. Food and Drug Administration (FDA) has approved NGENLA (somatrogon-ghla), a once-weekly, human growth hormone deficiency in the United States, continuing our commitment to helping children living with GHD may also experience challenges in relation to physical health and mental well-being. Growth hormone deficiency to combined pituitary hormone deficiency.

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