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Phenazopyridine Hydrochloride

NDC 51655-424 · Northwind Health Company, LLC

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

Packages

51655-424-27 — 12 TABLET in 1 BOTTLE, PLASTIC (51655-424-27)

51655-424-53 — 10 TABLET in 1 BOTTLE, PLASTIC (51655-424-53)

51655-424-87 — 6 TABLET in 1 BOTTLE, PLASTIC (51655-424-87)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49973-247 — Phenazopyridine Hydrochloride, 49973-301 — Urinary Pain Relief, 50090-5876 — Phenazopyridine, 50090-5904 — Phenazopyridine, 50090-6442 — Phenazopyridine, 50090-6951 — Phenazopyridine Hydrochloride, 50090-6952 — Phenazopyridine Hydrochloride, 50090-7291 — Phenazopyridine Hydrochloride, 50696-003 — Phenazopyridine Hydrochloride, 51655-007 — Phenazopyridine, 52389-241 — Phenazopyridine Hydochloride, 53943-336 — PHENAZOPYRIDINE HYDROCHLORIDE, 55319-211 — PHENAZOPYRIDINE HYDROCHLORIDE, 55910-631 — PHENAZOPYRIDINE HYDROCHLORIDE, 57237-330 — Phenazopyridine Hydrochloride, 57237-331 — Phenazopyridine Hydrochloride, 60846-501 — Phenazopyridine, 60846-502 — Phenazopyridine, 62011-0325 — PHENAZOPYRIDINE HYDROCHLORIDE, 62011-0412 — 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.