NDC 71209-080 – Olmesartan Medoxomil

Olmesartan Medoxomil 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71209-080

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Cadila Pharmaceuticals Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA210682
Marketed since
January 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan Medoxomil →

Package NDC codes (3)

Package NDCDescriptionSince
71209-080-0130 TABLET, COATED in 1 BOTTLE (71209-080-01)Jan 1, 2025
71209-080-0490 TABLET, COATED in 1 BOTTLE (71209-080-04)Jan 1, 2025
71209-080-10500 TABLET, COATED in 1 BOTTLE (71209-080-10)Jan 1, 2025

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