NDC 71610-837 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71610-837

Product details

Brand name
Metformin Hydrochloride
Generic name
metformin hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201991
Marketed since
March 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71610-837-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-30)May 31, 2024
71610-837-5360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-53)May 31, 2024
71610-837-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-60)May 31, 2024
71610-837-70120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-70)May 31, 2024
71610-837-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-80)May 31, 2024
71610-837-94360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-94)May 31, 2024

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