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
- 82804-047_8c3cb5d2-5e01-4f80-a8b8-70802ac0c8d6
- Product NDC
- 82804-047
- Form
- TABLET
- Composition / generic term
- Phenazopyridine Hydrochloride
- Labeler
- Proficient Rx LP
- 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
- 6 TABLET in 1 BOTTLE (82804-047-06) · 82804-047-06
- 10 TABLET in 1 BOTTLE (82804-047-10) · 82804-047-10
- 12 TABLET in 1 BOTTLE (82804-047-12) · 82804-047-12
- 18 TABLET in 1 BOTTLE (82804-047-18) · 82804-047-18
- 20 TABLET in 1 BOTTLE (82804-047-20) · 82804-047-20
- 24 TABLET in 1 BOTTLE (82804-047-24) · 82804-047-24
- 30 TABLET in 1 BOTTLE (82804-047-30) · 82804-047-30
- 60 TABLET in 1 BOTTLE (82804-047-60) · 82804-047-60
- 90 TABLET in 1 BOTTLE (82804-047-90) · 82804-047-90
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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