NDC 67877-218 – Metformin Hydrochloride

Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC67877-218

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091184
Marketed since
January 31, 2011
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
67877-218-01100 TABLET, FILM COATED in 1 BOTTLE (67877-218-01)Jan 31, 2011
67877-218-05500 TABLET, FILM COATED in 1 BOTTLE (67877-218-05)Jan 31, 2011
67877-218-101000 TABLET, FILM COATED in 1 BOTTLE (67877-218-10)Jan 31, 2011
67877-218-3810 BLISTER PACK in 1 CARTON (67877-218-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-218-33)Jan 31, 2011

Recalls mentioning this NDC

Other Metformin hydrochloride products