NDC 71335-0833 – Amlodipine besylate

Amlodipine Besylate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0833

Product details

Brand name
Amlodipine besylate
Generic name
Amlodipine besylate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077955
Marketed since
November 2, 2007
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 (7)

Package NDCDescriptionSince
71335-0833-130 TABLET in 1 BOTTLE (71335-0833-1)Oct 10, 2018
71335-0833-290 TABLET in 1 BOTTLE (71335-0833-2)May 16, 2018
71335-0833-3120 TABLET in 1 BOTTLE (71335-0833-3)Dec 27, 2021
71335-0833-460 TABLET in 1 BOTTLE (71335-0833-4)Oct 2, 2019
71335-0833-5500 TABLET in 1 BOTTLE (71335-0833-5)May 11, 2018
71335-0833-610 TABLET in 1 BOTTLE (71335-0833-6)Dec 27, 2021
71335-0833-7100 TABLET in 1 BOTTLE (71335-0833-7)Apr 4, 2024

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