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
- 70518-0218_55019fa1-bdb4-d578-e063-6294a90aa15d
- Product NDC
- 70518-0218
- Form
- TABLET
- Composition / generic term
- Phenazopyridine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20170214
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE, PLASTIC (70518-0218-0) · 70518-0218-0
- 12 TABLET in 1 BOTTLE, PLASTIC (70518-0218-3) · 70518-0218-3
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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