NDC 46708-215 – Amlodipine besylate and Olmesartran medoxomil

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

Human Prescription Drug

Product NDC46708-215

Product details

Brand name
Amlodipine besylate and Olmesartran medoxomil
Generic name
Amlodipine besylate and Olmesartran medoxomil
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207073
Marketed since
July 18, 2017
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 besylate and Olmesartran medoxomil →

Package NDC codes (3)

Package NDCDescriptionSince
46708-215-3030 TABLET, FILM COATED in 1 BOTTLE (46708-215-30)Jul 18, 2017
46708-215-9090 TABLET, FILM COATED in 1 BOTTLE (46708-215-90)Jul 18, 2017
46708-215-911000 TABLET, FILM COATED in 1 BOTTLE (46708-215-91)Jul 18, 2017

Other Amlodipine besylate and Olmesartran medoxomil products