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Azilsartan medoxomil

Azilsartan medoxomil · AZILSARTAN MEDOXOMIL 80 mg/1 · Tablet · Takeda Ireland Limited

NDC 66332-2003-01 · 30000 TABLET in 1 DRUM · DRUG FOR FURTHER PROCESSING · View full market →

Bulk ingredient — not a finished product

This NDC is a raw material (drug for further processing) sold to drug manufacturers or compounders, not a product pharmacies dispense. Retail pricing, TE codes, fragility scores, and shortage reports don't apply to bulk listings — those attach to finished products made from this ingredient.

Medicare Part D

This is a bulk ingredient, not a dispensable product — it is a raw material sold to manufacturers and compounders, so no plan prices it.

How Part D pricing works →

NADAC price per unit

No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.

Supply fragility

Not scored — fragility is computed for NADAC-priced NDCs.

Regulatory

Application
TE code
Approval date
Patents / exclusivity

Shortage history

No FDA shortage reports for this drug or its presentations.

Recalls (this NDC)

No enforcement reports list this package NDC.

Manufacturers of Azilsartan medoxomil (Tablet)

LabelerStrengthFirst seenLast seen
Lupin Pharmaceuticals, Inc.AZILSARTAN KAMEDOXOMIL 40 mg/1Jul 15, 2026Sep 2, 2026
Lupin Pharmaceuticals, Inc.AZILSARTAN KAMEDOXOMIL 80 mg/1Jul 15, 2026Sep 2, 2026
Takeda Ireland LimitedAZILSARTAN MEDOXOMIL 40 mg/1Jul 15, 2026Sep 2, 2026
Takeda Ireland LimitedAZILSARTAN MEDOXOMIL 80 mg/1Jul 15, 2026Sep 2, 2026

Roster from daily NDC Directory diffs — first/last seen dates start July 2026.

Cite this page

DrugDashboards, "Azilsartan medoxomil — NDC 66332-2003-01," retrieved September 3, 2026, https://drugdashboards.com/drug/66332200301.

Free to cite with attribution — see how the data is put together.