NDC 72789-514 – Amlodipine Besylate

Amlodipine Besylate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-514

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine Besylate
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076719
Marketed since
May 23, 2007
Listing expires
December 31, 2027
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
72789-514-3030 TABLET in 1 BOTTLE, PLASTIC (72789-514-30)May 5, 2026
72789-514-9090 TABLET in 1 BOTTLE, PLASTIC (72789-514-90)Mar 26, 2026
72789-514-951000 TABLET in 1 BOTTLE, PLASTIC (72789-514-95)Jun 26, 2025

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