NDC 23155-841 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-841

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213320
Marketed since
January 19, 2023
Marketing end
September 30, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
23155-841-01100 TABLET in 1 BOTTLE (23155-841-01)Jan 19, 2023
23155-841-05500 TABLET in 1 BOTTLE (23155-841-05)Jan 19, 2023
23155-841-101000 TABLET in 1 BOTTLE (23155-841-10)Aug 30, 2023

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