NDC 50090-7863 – Amlodipine and Olmesartan Medoxomil

Amlodipine Besylate 5 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7863

Product details

Brand name
Amlodipine and Olmesartan Medoxomil
Generic name
Amlodipine and Olmesartan Medoxomil
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206906
Marketed since
May 15, 2017
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50090-7863-030 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0)Jan 22, 2026

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