NDC 0480-7167 – Amlodipine Besylate

Amlodipine Besylate 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0480-7167

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine Besylate
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076846
Marketed since
October 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine besylate →

Package NDC codes (1)

Package NDCDescriptionSince
0480-7167-101000 TABLET in 1 BOTTLE (0480-7167-10)May 11, 2023

Other Amlodipine besylate products