NDC 67877-414 – Metformin Hydrochloride

Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC67877-414

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206145
Marketed since
October 27, 2018
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
67877-414-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-414-01)Oct 27, 2018
67877-414-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-414-05)Oct 27, 2018
67877-414-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-414-10)Oct 27, 2018
67877-414-3310 BLISTER PACK in 1 CARTON (67877-414-33) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKOct 27, 2018
67877-414-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-414-90)Dec 27, 2019

Recalls mentioning this NDC

Other Metformin hydrochloride products