NDC 71610-929 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71610-929

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077095
Marketed since
March 29, 2024
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
71610-929-3030 TABLET, FILM COATED in 1 BOTTLE (71610-929-30)Jul 22, 2025
71610-929-5360 TABLET, FILM COATED in 1 BOTTLE (71610-929-53)Jul 22, 2025
71610-929-6090 TABLET, FILM COATED in 1 BOTTLE (71610-929-60)Jul 22, 2025
71610-929-70120 TABLET, FILM COATED in 1 BOTTLE (71610-929-70)Jul 22, 2025
71610-929-80180 TABLET, FILM COATED in 1 BOTTLE (71610-929-80)Jul 22, 2025
71610-929-94360 TABLET, FILM COATED in 1 BOTTLE (71610-929-94)Jul 22, 2025

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