Skip to main content

Phenazopyridine Hydrochloride

NDC 69367-612 · Westminster Pharmaceuticals, LLC

Generic namePhenazopyridine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENAZOPYRIDINE HYDROCHLORIDE
Strength200 mg/1
Marketing categoryUNAPPROVED DRUG OTHER

Packages

69367-612-01 — 100 TABLET in 1 BOTTLE (69367-612-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2479 — Phenazopyridine, 68071-5302 — Phenazopyridine Hydrochloride, 68071-5309 — Phenazopyridine Hydrochloride, 68788-7778 — PHENAZOPYRIDINE HYDROCHLORIDE, 68788-7902 — Phenazopyridine, 68788-7981 — Phenazopyridine, 68788-8668 — Phenazopyridine Hydrochloride, 68788-8695 — Phenazopyridine Hydrochloride, 69256-767 — PHENAZOPYRIDINE HYDROCHLORIDE, 69367-611 — Phenazopyridine Hydrochloride, 69693-514 — Phenazopyridine hydrochloride, 69693-519 — Cystex Max Strength UTI Pain Relief, 69842-713 — PHENAZOPYRIDINE HYDROCHLORIDE, 70000-0241 — PHENAZOPYRIDINE HYDROCHLORIDE, 70000-0243 — PHENAZOPYRIDINE HYDROCHLORIDE, 70000-0523 — PHENAZOPYRIDINE HYDROCHLORIDE, 70518-0218 — Phenazopyridine Hydrochloride, 70518-3443 — Phenazopyridine, 70518-3868 — Phenazopyridine, 70518-3975 — Phenazopyridine Hydrochloride, +94 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.