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
- 71335-2323_f4ccf1f2-79d0-484a-802b-1ab625c1cb7e
- Product NDC
- 71335-2323
- Form
- TABLET
- Composition / generic term
- Phenazopyridine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20231019
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-2323-1) · 71335-2323-1
- 12 TABLET in 1 BOTTLE (71335-2323-2) · 71335-2323-2
- 9 TABLET in 1 BOTTLE (71335-2323-3) · 71335-2323-3
- 10 TABLET in 1 BOTTLE (71335-2323-4) · 71335-2323-4
- 15 TABLET in 1 BOTTLE (71335-2323-5) · 71335-2323-5
- 100 TABLET in 1 BOTTLE (71335-2323-6) · 71335-2323-6
- 6 TABLET in 1 BOTTLE (71335-2323-7) · 71335-2323-7
- 21 TABLET in 1 BOTTLE (71335-2323-8) · 71335-2323-8
- 30 TABLET in 1 BOTTLE (71335-2323-9) · 71335-2323-9
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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