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
- 71335-2321_55b0c95f-c150-418a-83a9-1708a517d1f5
- Product NDC
- 71335-2321
- 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 — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 TABLET in 1 BOTTLE (71335-2321-1) · 71335-2321-1
- 20 TABLET in 1 BOTTLE (71335-2321-2) · 71335-2321-2
- 30 TABLET in 1 BOTTLE (71335-2321-3) · 71335-2321-3
- 10 TABLET in 1 BOTTLE (71335-2321-4) · 71335-2321-4
- 15 TABLET in 1 BOTTLE (71335-2321-5) · 71335-2321-5
- 6 TABLET in 1 BOTTLE (71335-2321-6) · 71335-2321-6
- 90 TABLET in 1 BOTTLE (71335-2321-7) · 71335-2321-7
- 12 TABLET in 1 BOTTLE (71335-2321-8) · 71335-2321-8
- 18 TABLET in 1 BOTTLE (71335-2321-9) · 71335-2321-9
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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