NDC 71610-533 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71610-533

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 · ANDA078321
Marketed since
April 17, 2008
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
71610-533-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-533-30)Apr 15, 2021
71610-533-5360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-533-53)Mar 9, 2021
71610-533-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-533-60)Apr 15, 2021
71610-533-70120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-533-70)May 18, 2021
71610-533-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-533-80)May 18, 2021

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