NDC 67877-199 – Amlodipine Besylate

Amlodipine Besylate 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC67877-199

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
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 (4)

Package NDCDescriptionSince
67877-199-05500 TABLET in 1 BOTTLE (67877-199-05)Oct 20, 2010
67877-199-101000 TABLET in 1 BOTTLE (67877-199-10)Oct 20, 2010
67877-199-3810 BLISTER PACK in 1 CARTON (67877-199-38) / 10 TABLET in 1 BLISTER PACKOct 20, 2010
67877-199-9090 TABLET in 1 BOTTLE (67877-199-90)Oct 20, 2010

Recalls mentioning this NDC

Other Amlodipine besylate products