FDA NDC Directory · JSON-LD · Markdown

PHENAZOPYRIDINE HYDROCHLORIDE

NDC 64950-551 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGenus Lifesciences Inc.
Marketing categoryUnapproved drug (not FDA-reviewed)
Dosage form / routeTABLET · ORAL
Active ingredientsPHENAZOPYRIDINE HYDROCHLORIDE (200 mg/1)
Marketing started20260608
Package count1

External sources

Source: openFDA. Public-domain (CC0).