NDC 69097-128 – Amlodipine Besylate

Amlodipine Besylate 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC69097-128

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine Besylate
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077073
Marketed since
September 26, 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 (2)

Package NDCDescriptionSince
69097-128-0590 TABLET in 1 BOTTLE (69097-128-05)Sep 26, 2007
69097-128-151000 TABLET in 1 BOTTLE (69097-128-15)Sep 26, 2007

Recalls mentioning this NDC

Other Amlodipine besylate products