United States · FDA National Drug Code directory
Methenamine Mandelate
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
- 69367-436_6e6f983d-9926-4c26-afc1-0946184911d1
- Product NDC
- 69367-436
- Form
- TABLET, FILM COATED
- Composition / generic term
- Methenamine Mandelate
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20260319
- Source listing expiry
- 20271231
Source-listed ingredients
- METHENAMINE MANDELATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (69367-436-01) · 69367-436-01
- 60 TABLET, FILM COATED in 1 BOTTLE (69367-436-60) · 69367-436-60
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 →