NDC 42291-004 – Amlodipine and Olmesartan Medoxomil

Amlodipine Besylate 10 mg/1; Olmesartan Medoxomil 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC42291-004

Product details

Brand name
Amlodipine and Olmesartan Medoxomil
Generic name
Amlodipine and Olmesartan Medoxomil
Labeler
AvKARE
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209010
Marketed since
June 18, 2024
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
42291-004-3030 TABLET, FILM COATED in 1 BOTTLE (42291-004-30)Jun 18, 2024

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