NDC 68382-122 – Amlodipine Besylate

Amlodipine Besylate 5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68382-122

Product details

Brand name
Amlodipine Besylate
Generic name
Amlodipine Besylate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078226
Marketed since
September 21, 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 (4)

Package NDCDescriptionSince
68382-122-01100 TABLET in 1 BOTTLE (68382-122-01)Sep 21, 2007
68382-122-05500 TABLET in 1 BOTTLE (68382-122-05)Sep 21, 2007
68382-122-1690 TABLET in 1 BOTTLE (68382-122-16)Sep 21, 2007
68382-122-7710 BLISTER PACK in 1 CARTON (68382-122-77) / 10 TABLET in 1 BLISTER PACKSep 21, 2007

Recalls mentioning this NDC

Other Amlodipine besylate products