NDC 49483-623 – Metformin Hydrochloride Extended Release

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

Human Prescription Drug 3 recalls

Product NDC49483-623

Product details

Brand name
Metformin Hydrochloride Extended Release
Generic name
Metformin Hydrochloride
Labeler
TIME CAP LABORATORIES, INC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090295
Marketed since
May 12, 2016
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin Hydrochloride Extended Release →

Package NDC codes (4)

Package NDCDescriptionSince
49483-623-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49483-623-01)Jun 28, 2016
49483-623-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49483-623-09)Jun 5, 2017
49483-623-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49483-623-10)Jun 5, 2017
49483-623-50500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49483-623-50)Jun 28, 2016

Recalls mentioning this NDC

Other Metformin Hydrochloride Extended Release products