NDC 69238-2126 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC69238-2126

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078596
Marketed since
February 26, 2010
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
69238-2126-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-1)Feb 26, 2010
69238-2126-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-3)Feb 26, 2010
69238-2126-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-5)Feb 26, 2010
69238-2126-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-9)Feb 26, 2010

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