United States · FDA National Drug Code directory
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
- 0378-0213_21d4a0c6-4112-42bd-8738-2df8d81debf1
- Product NDC
- 0378-0213
- Form
- TABLET
- Composition / generic term
- chlorthalidone
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19810226
- Source listing expiry
- 20271231
Source-listed ingredients
- CHLORTHALIDONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0378-0213-01) · 0378-0213-01
- 1000 TABLET in 1 BOTTLE (0378-0213-10) · 0378-0213-10
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 →