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
- 70518-3975_5796d1de-ee8d-ba66-e063-6294a90afca2
- Product NDC
- 70518-3975
- Form
- TABLET
- Composition / generic term
- Phenazopyridine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20240106
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BLISTER PACK (70518-3975-0) · 70518-3975-0
- 9 TABLET in 1 BOTTLE, PLASTIC (70518-3975-2) · 70518-3975-2
- 6 TABLET in 1 BOTTLE, PLASTIC (70518-3975-3) · 70518-3975-3
- 50 POUCH in 1 BOX (70518-3975-4) / 1 TABLET in 1 POUCH (70518-3975-5) · 70518-3975-4
- 100 POUCH in 1 BOX (70518-3975-6) / 1 TABLET in 1 POUCH (70518-3975-5) · 70518-3975-6
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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