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
- 50090-5876_ab18cf45-4c1d-4d6a-9195-e70ad6e0cd68
- Product NDC
- 50090-5876
- Form
- TABLET
- Composition / generic term
- Phenazopyridine
- Labeler
- A-S Medication Solutions
- 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
- 10 TABLET in 1 BOTTLE (50090-5876-0) · 50090-5876-0
- 15 TABLET in 1 BOTTLE (50090-5876-1) · 50090-5876-1
- 6 TABLET in 1 BOTTLE (50090-5876-4) · 50090-5876-4
- 12 TABLET in 1 BOTTLE (50090-5876-6) · 50090-5876-6
- 9 TABLET in 1 BOTTLE (50090-5876-7) · 50090-5876-7
- 21 TABLET in 1 BOTTLE (50090-5876-8) · 50090-5876-8
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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