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
- 65841-806_9e0aa50a-1fac-4086-b7b6-811cec3f524b
- Product NDC
- 65841-806
- Form
- TABLET
- Composition / generic term
- telmisartan
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140827
- Source listing expiry
- 20261231
Source-listed ingredients
- TELMISARTAN — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (65841-806-01) · 65841-806-01
- 500 TABLET in 1 BOTTLE (65841-806-05) · 65841-806-05
- 30 TABLET in 1 BOTTLE (65841-806-06) · 65841-806-06
- 1000 TABLET in 1 BOTTLE (65841-806-10) · 65841-806-10
- 90 TABLET in 1 BOTTLE (65841-806-16) · 65841-806-16
- 30 BLISTER PACK in 1 CARTON (65841-806-78) / 1 TABLET in 1 BLISTER PACK (65841-806-30) · 65841-806-78
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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