NDC 71610-587 – Metformin hydrochloride

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

Human Prescription Drug

Product NDC71610-587

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 · ANDA207427
Marketed since
July 17, 2018
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
71610-587-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-30)Jan 18, 2022
71610-587-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-60)Jul 28, 2021
71610-587-70120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-70)Jul 28, 2021
71610-587-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-80)Jul 28, 2021
71610-587-92270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-92)Jan 18, 2022
71610-587-94360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-587-94)Jul 28, 2021

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