NDC 71335-0843 – Amlodipine besylate

Amlodipine Besylate 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0843

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 (10)

Package NDCDescriptionSince
71335-0843-07 TABLET in 1 BOTTLE (71335-0843-0)Apr 4, 2024
71335-0843-130 TABLET in 1 BOTTLE (71335-0843-1)Feb 23, 2022
71335-0843-290 TABLET in 1 BOTTLE (71335-0843-2)Feb 23, 2022
71335-0843-360 TABLET in 1 BOTTLE (71335-0843-3)Feb 23, 2022
71335-0843-4120 TABLET in 1 BOTTLE (71335-0843-4)Feb 23, 2022
71335-0843-5100 TABLET in 1 BOTTLE (71335-0843-5)Feb 23, 2022
71335-0843-6800 TABLET in 1 BOTTLE (71335-0843-6)Feb 23, 2022
71335-0843-71000 TABLET in 1 BOTTLE (71335-0843-7)Feb 23, 2022
71335-0843-8180 TABLET in 1 BOTTLE (71335-0843-8)Feb 23, 2022
71335-0843-910 TABLET in 1 BOTTLE (71335-0843-9)Feb 23, 2022

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