NDC 69238-2125 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC69238-2125

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
December 2, 2009
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
69238-2125-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2125-1)Dec 2, 2009
69238-2125-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2125-3)Dec 2, 2009
69238-2125-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2125-5)Dec 2, 2009
69238-2125-71000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2125-7)Dec 2, 2009
69238-2125-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2125-9)Dec 2, 2009

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