NDC 71610-917 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-917

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203769
Marketed since
February 1, 2015
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71610-917-3030 TABLET in 1 BOTTLE (71610-917-30)Jun 26, 2025
71610-917-5360 TABLET in 1 BOTTLE (71610-917-53)Jun 26, 2025
71610-917-6090 TABLET in 1 BOTTLE (71610-917-60)Jun 26, 2025
71610-917-70120 TABLET in 1 BOTTLE (71610-917-70)Jun 26, 2025
71610-917-80180 TABLET in 1 BOTTLE (71610-917-80)Jun 26, 2025
71610-917-92270 TABLET in 1 BOTTLE (71610-917-92)Mar 25, 2026
71610-917-94360 TABLET in 1 BOTTLE (71610-917-94)Jun 26, 2025

Other Metformin hydrochloride products