NDC 71335-0890 – Amlodipine Besylate

Amlodipine Besylate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0890

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine besylate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078925
Marketed since
October 20, 2010
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 (8)

Package NDCDescriptionSince
71335-0890-130 TABLET in 1 BOTTLE (71335-0890-1)Mar 7, 2019
71335-0890-290 TABLET in 1 BOTTLE (71335-0890-2)Jul 2, 2018
71335-0890-3120 TABLET in 1 BOTTLE (71335-0890-3)Nov 8, 2023
71335-0890-460 TABLET in 1 BOTTLE (71335-0890-4)Nov 7, 2018
71335-0890-5500 TABLET in 1 BOTTLE (71335-0890-5)Jul 23, 2024
71335-0890-610 TABLET in 1 BOTTLE (71335-0890-6)Jul 23, 2024
71335-0890-7100 TABLET in 1 BOTTLE (71335-0890-7)Jul 23, 2024
71335-0890-8180 TABLET in 1 BOTTLE (71335-0890-8)Jul 23, 2024

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