AZO

NDC 49973-301 · i-Health, Inc.

Generic nameUrinary Pain Relief

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENAZOPYRIDINE HYDROCHLORIDE

Strength95 mg/1

Marketing categoryUNAPPROVED DRUG OTHER

Packages

49973-301-31 — 15 BLISTER PACK in 1 BOX (49973-301-31) / 2 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-756 — Phenazopyridine Hydrochloride, 36800-040 — PHENAZOPYRIDINE HYDROCHLORIDE, 36800-510 — PHENAZOPYRIDINE HYDROCHLORIDE, 37012-098 — PHENAZOPYRIDINE HYDROCHLORIDE, 41250-342 — PHENAZOPYRIDINE HYDROCHLORIDE, 46122-337 — PHENAZOPYRIDINE HYDROCHLORIDE, 46122-628 — PHENAZOPYRIDINE HYDROCHLORIDE, 49035-297 — PHENAZOPYRIDINE HYDROCHLORIDE, 49348-076 — PHENAZOPYRIDINE HYDROCHLORIDE, 49973-247 — Phenazopyridine Hydrochloride, 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, 51655-424 — Phenazopyridine, 52389-241 — Phenazopyridine Hydochloride, +94 more

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