Package 70518-4369-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4369-0
Digits Only 7051843690
Product NDC 70518-4369
Product ID 70518-4369_3852dad0-7b83-5c22-e063-6294a90aa2aa
Description

30 POUCH in 1 BOX (70518-4369-0) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-4369-1)

Marketing

Marketing Status
Marketed Since 2025-06-24
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3852dad0-7b83-5c22-e063-6294a90aa2aa", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807894"], "spl_set_id": ["d5228e81-9c86-4781-b984-20feaa2ae779"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4369-0)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-4369-1)", "package_ndc": "70518-4369-0", "marketing_start_date": "20250624"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-4369_3852dad0-7b83-5c22-e063-6294a90aa2aa", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-4369", "generic_name": "Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA090692", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}