Skip to main content

Phenazopyridine Hydrochloride

NDC 68788-8695 · Preferred Pharmaceuticals Inc

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

Packages

68788-8695-1 — 15 TABLET in 1 BOTTLE (68788-8695-1)

68788-8695-9 — 9 TABLET in 1 BOTTLE (68788-8695-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68016-129 — PHENAZOPYRIDINE HYDROCHLORIDE, 68071-2273 — PHENAZOPYRIDINE HYDROCHLORIDE, 68071-2357 — Phenazopyridine, 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, 69256-767 — PHENAZOPYRIDINE HYDROCHLORIDE, 69367-611 — Phenazopyridine Hydrochloride, 69367-612 — 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, +94 more

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