United States · FDA National Drug Code directory
Candesartan Cilexetil and Hydrochlorothiazide
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
- 33342-131_07873250-a90d-4e06-bfa8-a4202794791d
- Product NDC
- 33342-131
- Form
- TABLET
- Composition / generic term
- Candesartan Cilexetil and Hydrochlorothiazide
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150307
- Source listing expiry
- 20271231
Source-listed ingredients
- CANDESARTAN CILEXETIL — 16 mg/1
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (33342-131-10) · 33342-131-10
- 10 BLISTER PACK in 1 CARTON (33342-131-12) / 10 TABLET in 1 BLISTER PACK · 33342-131-12
- 500 TABLET in 1 BOTTLE (33342-131-15) · 33342-131-15
- 300 TABLET in 1 BOTTLE (33342-131-51) · 33342-131-51
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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