United States · FDA National Drug Code directory
CHLORTHALIDONE CHLORTHALIDONE
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
- 62332-676_56256d08-66bc-4424-84d4-2db217e5f4d6
- Product NDC
- 62332-676
- Form
- TABLET
- Composition / generic term
- CHLORTHALIDONE
- Labeler
- Alembic Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220829
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORTHALIDONE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (62332-676-31) · 62332-676-31
- 90 TABLET in 1 BOTTLE (62332-676-90) · 62332-676-90
- 1000 TABLET in 1 BOTTLE (62332-676-91) · 62332-676-91
Source and coverage
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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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