NDC 71335-2359 – Amlodipine Besylate

Amlodipine Besylate 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2359

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine Besylate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203245
Marketed since
May 22, 2019
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
71335-2359-05 TABLET in 1 BOTTLE, PLASTIC (71335-2359-0)Mar 5, 2024
71335-2359-130 TABLET in 1 BOTTLE, PLASTIC (71335-2359-1)Mar 5, 2024
71335-2359-290 TABLET in 1 BOTTLE, PLASTIC (71335-2359-2)Mar 5, 2024
71335-2359-360 TABLET in 1 BOTTLE, PLASTIC (71335-2359-3)Mar 5, 2024
71335-2359-4100 TABLET in 1 BOTTLE, PLASTIC (71335-2359-4)Mar 5, 2024
71335-2359-5180 TABLET in 1 BOTTLE, PLASTIC (71335-2359-5)Mar 5, 2024
71335-2359-6120 TABLET in 1 BOTTLE, PLASTIC (71335-2359-6)Mar 5, 2024
71335-2359-710 TABLET in 1 BOTTLE, PLASTIC (71335-2359-7)Mar 5, 2024
71335-2359-8500 TABLET in 1 BOTTLE, PLASTIC (71335-2359-8)Mar 5, 2024
71335-2359-91000 TABLET in 1 BOTTLE, PLASTIC (71335-2359-9)Mar 5, 2024

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