NDC 25000-101 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC25000-101

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
MARKSANS PHARMA LIMITED
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 →

Package NDC codes (5)

Package NDCDescriptionSince
25000-101-0330 TABLET, EXTENDED RELEASE in 1 BOTTLE (25000-101-03)May 12, 2016
25000-101-12500 TABLET, EXTENDED RELEASE in 1 BOTTLE (25000-101-12)May 12, 2016
25000-101-141000 TABLET, EXTENDED RELEASE in 1 BOTTLE (25000-101-14)Jun 24, 2022
25000-101-974 BAG in 1 BOX (25000-101-97) / 2000 TABLET, EXTENDED RELEASE in 1 BAGMay 12, 2016
25000-101-981 BAG in 1 BOX (25000-101-98) / 11695 TABLET, EXTENDED RELEASE in 1 BAGMay 12, 2016

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