NDC 50090-6686 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC50090-6686

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203281
Marketed since
May 25, 2017
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50090-6686-090 TABLET, FILM COATED in 1 BOTTLE (50090-6686-0)Sep 15, 2023

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