NDC 68788-8866 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC68788-8866

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA217631
Marketed since
April 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
68788-8866-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-1)Apr 23, 2025
68788-8866-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-3)Apr 23, 2025
68788-8866-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-6)Apr 23, 2025
68788-8866-8120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-8)Apr 23, 2025
68788-8866-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-9)Apr 23, 2025

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