FDA NDC Directory · JSON-LD · Markdown

Phenylephrine Hydrochloride

NDC 70069-591 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215617
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsPHENYLEPHRINE HYDROCHLORIDE (.1 mg/mL)
Marketing started20250304
Package count1

External sources

Source: openFDA. Public-domain (CC0).