United States · FDA National Drug Code directory
IRBESARTAN
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
- 42658-122_5844e955-a63d-6fb4-e063-6294a90a3caa
- Product NDC
- 42658-122
- Form
- TABLET, FILM COATED
- Composition / generic term
- IRBESARTAN
- Labeler
- Hisun Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170415
- Source listing expiry
- 20271231
Source-listed ingredients
- IRBESARTAN — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (42658-122-01) · 42658-122-01
- 90 TABLET, FILM COATED in 1 BOTTLE (42658-122-04) · 42658-122-04
- 500 TABLET, FILM COATED in 1 BOTTLE (42658-122-07) · 42658-122-07
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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