United States · FDA National Drug Code directory
Telmisartan and Amlodipine
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
- 68180-196_17a6182b-5050-470e-aa1d-1605fa9e088e
- Product NDC
- 68180-196
- Form
- TABLET
- Composition / generic term
- Telmisartan and Amlodipine
- Labeler
- Lupin Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140108
- Source listing expiry
- 20261231
Source-listed ingredients
- TELMISARTAN — 40 mg/1
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
Package details are not available in this snapshot.
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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