United States · FDA National Drug Code directory

Azilsartan medoxomil

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
70748-237_f05aba4d-376f-460f-9264-ecf267e04dcd
Product NDC
70748-237
Form
TABLET
Composition / generic term
Azilsartan medoxomil
Labeler
Lupin Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260514
Source listing expiry
20271231

Source-listed ingredients

  • AZILSARTAN KAMEDOXOMIL — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (70748-237-06) · 70748-237-06

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 →