United States · FDA National Drug Code directory

Metolazone

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
50742-350_40a518ac-5d45-4c61-e063-6294a90a6ec9
Product NDC
50742-350
Form
TABLET
Composition / generic term
Metolazone
Labeler
Ingenus Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20230124
Source listing expiry
20261231

Source-listed ingredients

  • METOLAZONE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (50742-350-01) · 50742-350-01

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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