United States · FDA National Drug Code directory

Phenazopyridine Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 70518-3986_59912492-11ce-ff33-e063-6394a90ac2cf
Product NDC: 70518-3986
Form: TABLET
Composition / generic term: Phenazopyridine Hydrochloride
Labeler: REMEDYREPACK INC.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start / end (source format): 20240115
Source listing expiry: 20271231

Source-listed ingredients

PHENAZOPYRIDINE HYDROCHLORIDE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BLISTER PACK (70518-3986-0) · 70518-3986-0
12 TABLET in 1 BOTTLE, PLASTIC (70518-3986-1) · 70518-3986-1
6 TABLET in 1 BOTTLE, PLASTIC (70518-3986-2) · 70518-3986-2
50 POUCH in 1 BOX (70518-3986-3) / 1 TABLET in 1 POUCH (70518-3986-4) · 70518-3986-3
100 POUCH in 1 BOX (70518-3986-5) / 1 TABLET in 1 POUCH (70518-3986-4) · 70518-3986-5

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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