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Phenazopyridine Hydrochloride

NDC 68071-2357 · NuCare Pharmaceuticals,Inc.

Generic namePhenazopyridine
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENAZOPYRIDINE HYDROCHLORIDE
Strength100 mg/1
Marketing categoryUNAPPROVED DRUG OTHER

Packages

68071-2357-2 — 12 TABLET in 1 BOTTLE (68071-2357-2)

68071-2357-4 — 4 TABLET in 1 BOTTLE (68071-2357-4)

68071-2357-8 — 8 TABLET in 1 BOTTLE (68071-2357-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63736-020 — Phenazopyridine hydrochloride, 63868-117 — PHENAZOPYRIDINE HYDROCHLORIDE, 63868-297 — PHENAZOPYRIDINE HYDROCHLORIDE, 64950-550 — PHENAZOPYRIDINE HYDROCHLORIDE, 64950-551 — PHENAZOPYRIDINE HYDROCHLORIDE, 65162-681 — Phenazopyridine, 65162-682 — Phenazopyridine, 67296-2206 — Phenazopyridine Hydrochloride, 68016-129 — PHENAZOPYRIDINE HYDROCHLORIDE, 68071-2273 — PHENAZOPYRIDINE HYDROCHLORIDE, 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, +94 more

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