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
- 65162-293_1a0e1325-40d8-4dde-8655-54f6bd962a4f
- Product NDC
- 65162-293
- Form
- TABLET
- Composition / generic term
- Telmisartan
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130531
- Source listing expiry
- 20261231
Source-listed ingredients
- TELMISARTAN — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (65162-293-03) · 65162-293-03
- 90 TABLET in 1 BOTTLE (65162-293-09) · 65162-293-09
- 1000 TABLET in 1 BOTTLE (65162-293-11) · 65162-293-11
- 500 TABLET in 1 BOTTLE (65162-293-50) · 65162-293-50
- 3 BLISTER PACK in 1 CARTON (65162-293-63) / 10 TABLET in 1 BLISTER PACK · 65162-293-63
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 →