NDC 10135-823 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC10135-823

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202306
Marketed since
September 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
10135-823-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-05)Sep 1, 2026
10135-823-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-10)Sep 1, 2026
10135-823-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-30)Sep 1, 2026
10135-823-32180 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-32)Sep 1, 2026
10135-823-33360 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-33)Sep 1, 2026
10135-823-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-60)Sep 1, 2026
10135-823-62120 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-62)Sep 1, 2026
10135-823-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-90)Sep 1, 2026

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