NDC 71335-2504 – Metformin Hydrochloride

Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2504

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078321
Marketed since
February 15, 2024
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-2504-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2504-1)Sep 23, 2024
71335-2504-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2504-2)Sep 23, 2024
71335-2504-360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2504-3)Sep 23, 2024
71335-2504-4180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2504-4)Sep 23, 2024
71335-2504-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2504-5)Sep 23, 2024

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