Phenazopyridine Hydrochloride

NDC 68788-7902 · Preferred Pharmaceuticals Inc.

Generic namePhenazopyridine

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENAZOPYRIDINE HYDROCHLORIDE

Strength200 mg/1

Marketing categoryUNAPPROVED DRUG OTHER

Packages

68788-7902-1 — 15 TABLET in 1 BOTTLE (68788-7902-1)

68788-7902-9 — 9 TABLET in 1 BOTTLE (68788-7902-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65162-681 — Phenazopyridine, 65162-682 — Phenazopyridine, 67296-2206 — Phenazopyridine Hydrochloride, 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, 68788-7981 — Phenazopyridine, 68788-8668 — Phenazopyridine Hydrochloride, 68788-8695 — 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, +94 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.