United States · FDA National Drug Code directory

Telmisartan

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
33342-120_94abae59-69ec-482d-b4cf-285d502d82e7
Product NDC
33342-120
Form
TABLET
Composition / generic term
Telmisartan
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20250115
Source listing expiry
20271231

Source-listed ingredients

  • TELMISARTAN — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 CONTAINER (33342-120-07) · 33342-120-07
  • 90 TABLET in 1 CONTAINER (33342-120-10) · 33342-120-10

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.

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