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
- 82804-995_ac155091-ee07-46da-bb25-ff4cd4074610
- Product NDC
- 82804-995
- 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 — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (82804-995-00) · 82804-995-00
- 6 TABLET in 1 BOTTLE (82804-995-06) · 82804-995-06
- 10 TABLET in 1 BOTTLE (82804-995-10) · 82804-995-10
- 12 TABLET in 1 BOTTLE (82804-995-12) · 82804-995-12
- 20 TABLET in 1 BOTTLE (82804-995-20) · 82804-995-20
- 24 TABLET in 1 BOTTLE (82804-995-24) · 82804-995-24
- 500 TABLET in 1 BOTTLE (82804-995-55) · 82804-995-55
- 90 TABLET in 1 BOTTLE (82804-995-90) · 82804-995-90
- 96 TABLET in 1 BOTTLE (82804-995-96) · 82804-995-96
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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