NDC 71610-652 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71610-652

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 · ANDA078596
Marketed since
March 28, 2022
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
71610-652-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-30)Jul 14, 2022
71610-652-5360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-53)Jul 14, 2022
71610-652-6090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-60)Jul 14, 2022
71610-652-70120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-70)Jul 14, 2022
71610-652-80180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-80)Jul 14, 2022
71610-652-94360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-652-94)Jul 14, 2022

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