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
- 68462-199_7e08eda5-be87-4e09-ae4e-880a18aa7a0b
- Product NDC
- 68462-199
- Form
- TABLET
- Composition / generic term
- Telmisartan
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140707
- Source listing expiry
- 20271231
Source-listed ingredients
- TELMISARTAN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68462-199-01) · 68462-199-01
- 3 BLISTER PACK in 1 CARTON (68462-199-13) / 10 TABLET in 1 BLISTER PACK · 68462-199-13
- 30 TABLET in 1 BOTTLE (68462-199-30) · 68462-199-30
- 90 TABLET in 1 BOTTLE (68462-199-90) · 68462-199-90
- 6 BLISTER PACK in 1 CARTON (68462-199-96) / 10 TABLET in 1 BLISTER PACK · 68462-199-96
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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