FDA NDC Directory · JSON-LD · Markdown

HYDROXYUREA

NDC 70069-820 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218021
Dosage form / routeCAPSULE · ORAL
Active ingredientsHYDROXYUREA (500 mg/1)
Marketing started20240618
Package count1

External sources

Source: openFDA. Public-domain (CC0).