FDA NDC Directory · JSON-LD · Markdown

PHENYLEPHRINE HYDROCHLORIDE

NDC 70069-802 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213318
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsPHENYLEPHRINE HYDROCHLORIDE (50 mg/5mL)
Marketing started20210922
Package count1

External sources

Source: openFDA. Public-domain (CC0).