NDC 50090-1494 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC50090-1494

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201991
Marketed since
March 1, 2013
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
50090-1494-060 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1494-0)Dec 4, 2014
50090-1494-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1494-1)Dec 4, 2014
50090-1494-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1494-2)Dec 4, 2014
50090-1494-3180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1494-3)Dec 4, 2014
50090-1494-4100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1494-4)Mar 12, 2024

Recalls mentioning this NDC

Other Metformin hydrochloride products