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
- 71205-813_e018e176-c4ec-42a2-9119-f1278cfa719a
- Product NDC
- 71205-813
- Form
- TABLET
- Composition / generic term
- Phenazopyridine
- Labeler
- Proficient Rx LP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20110201
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (71205-813-06) · 71205-813-06
- 10 TABLET in 1 BOTTLE (71205-813-10) · 71205-813-10
- 12 TABLET in 1 BOTTLE (71205-813-12) · 71205-813-12
- 20 TABLET in 1 BOTTLE (71205-813-20) · 71205-813-20
- 24 TABLET in 1 BOTTLE (71205-813-24) · 71205-813-24
- 30 TABLET in 1 BOTTLE (71205-813-30) · 71205-813-30
- 60 TABLET in 1 BOTTLE (71205-813-60) · 71205-813-60
- 90 TABLET in 1 BOTTLE (71205-813-90) · 71205-813-90
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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