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
50268-549_0e88fdee-dba1-56cd-e063-6394a90a47c6
Product NDC
50268-549
Form
TABLET
Composition / generic term
Methenamine Hippurate
Labeler
AvPAK
Marketing category
ANDA
Marketing start / end (source format)
20201202
Source listing expiry
20261231

Source-listed ingredients

  • METHENAMINE HIPPURATE — 1000 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 50 BLISTER PACK in 1 CARTON (50268-549-15) / 1 TABLET in 1 BLISTER PACK (50268-549-11) · 50268-549-15

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.

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