NDC 67877-901 – Amlodipine Besylate

Amlodipine Besylate 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67877-901

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine besylate
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078925
Marketed since
December 6, 2025
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 (3)

Package NDCDescriptionSince
67877-901-05500 TABLET in 1 BOTTLE (67877-901-05)May 21, 2026
67877-901-101000 TABLET in 1 BOTTLE (67877-901-10)Apr 1, 2026
67877-901-9090 TABLET in 1 BOTTLE (67877-901-90)Feb 1, 2026

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