NDC 51407-859 – amlodipine besylate and olmesartan medoxomil

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

Human Prescription Drug

Product NDC51407-859

Product details

Brand name
amlodipine besylate and olmesartan medoxomil
Generic name
amlodipine besylate and olmesartan medoxomil
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA022100
Marketed since
September 26, 2007
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 besylate and olmesartan medoxomil →

Package NDC codes (1)

Package NDCDescriptionSince
51407-859-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-859-30)May 13, 2024

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