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
- 68788-8668_a15c3b29-f4d7-4d47-8feb-d66ab9f3491d
- Product NDC
- 68788-8668
- Form
- TABLET
- Composition / generic term
- Phenazopyridine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20240520
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (68788-8668-1) · 68788-8668-1
- 6 TABLET in 1 BOTTLE (68788-8668-6) · 68788-8668-6
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →