NDC 69238-2676 – Amlodipine and Olmesartan Medoxomil

Amlodipine Besylate 5 mg/1; Olmesartan Medoxomil 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69238-2676

Product details

Brand name
Amlodipine and Olmesartan Medoxomil
Generic name
Amlodipine and Olmesartan Medoxomil
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209010
Marketed since
December 3, 2018
Listing expires
December 31, 2026
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
69238-2676-11000 TABLET, FILM COATED in 1 BOTTLE (69238-2676-1)Dec 3, 2018

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