United States · FDA National Drug Code directory
Methenamine Hippurate
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
- 42571-332_350168e0-c68a-6cfa-e063-6294a90ab7fe
- Product NDC
- 42571-332
- Form
- TABLET
- Composition / generic term
- Methenamine Hippurate
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190815
- Source listing expiry
- 20261231
Source-listed ingredients
- METHENAMINE HIPPURATE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (42571-332-01) · 42571-332-01
- 80 TABLET in 1 CARTON (42571-332-23) · 42571-332-23
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 →