Phenazopyridine Hydrochloride

NDC 70518-3443 · REMEDYREPACK INC.

Generic namePhenazopyridine

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENAZOPYRIDINE HYDROCHLORIDE

Strength100 mg/1

Marketing categoryUNAPPROVED DRUG OTHER

Packages

70518-3443-1 — 12 TABLET in 1 BOTTLE, PLASTIC (70518-3443-1)

70518-3443-3 — 6 TABLET in 1 BOTTLE, PLASTIC (70518-3443-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70518-3868 — Phenazopyridine, 70518-3975 — Phenazopyridine Hydrochloride, 70518-3986 — Phenazopyridine Hydrochloride, 70677-0078 — PHENAZOPYRIDINE HYDROCHLORIDE, 70677-1229 — PHENAZOPYRIDINE HYDROCHLORIDE, 70677-1230 — PHENAZOPYRIDINE HYDROCHLORIDE, 70692-163 — Phenazopyridine Hydrochloride, 70692-178 — Phenazopyridine hydrochloride, 71205-584 — PHENAZOPYRIDINE HYDROCHLORIDE, 71205-813 — Phenazopyridine, +94 more

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