Package 70518-2709-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2709-1
Digits Only 7051827091
Product NDC 70518-2709
Product ID 70518-2709_3996536a-978c-02cc-e063-6394a90a715b
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2709-1)

Marketing

Marketing Status
Marketed Since 2024-07-15
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3996536a-978c-02cc-e063-6394a90a715b", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["1503bbe4-0ac5-479b-9900-d38e49236bf0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2709-1)", "package_ndc": "70518-2709-1", "marketing_start_date": "20240715"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-2709_3996536a-978c-02cc-e063-6394a90a715b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-2709", "generic_name": "Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20200424", "listing_expiration_date": "20261231"}