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
62332-533_4e197913-c368-474d-a147-e9ade3021e37
Product NDC
62332-533
Form
TABLET
Composition / generic term
METOLAZONE
Labeler
Alembic Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20201202
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 (62332-533-31) · 62332-533-31
  • 1000 TABLET in 1 BOTTLE (62332-533-91) · 62332-533-91

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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