NDC 55111-320 – Glimepiride

Glimepiride 1 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC55111-320

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077091
Marketed since
October 6, 2005
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (4)

Package NDCDescriptionSince
55111-320-01100 TABLET in 1 BOTTLE (55111-320-01)Oct 6, 2005
55111-320-05500 TABLET in 1 BOTTLE (55111-320-05)Oct 6, 2005
55111-320-3030 TABLET in 1 BOTTLE (55111-320-30)Oct 6, 2005
55111-320-78100 BLISTER PACK in 1 CARTON (55111-320-78) / 1 TABLET in 1 BLISTER PACK (55111-320-79)Oct 6, 2005

Recalls mentioning this NDC

Other Glimepiride products