Package 70518-3130-1
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
70518-3130-1
Digits Only
7051831301
Product NDC
70518-3130
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3130-1)
Marketing
Marketing Status
Brand
metformin hydrochloride
Generic
metformin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e73d3eb-ffa7-6f9c-e063-6294a90a8666", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["5d8d654a-9bb4-4c87-ab43-c21c4e874708"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3130-1)", "package_ndc": "70518-3130-1", "marketing_start_date": "20250422"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3130-2)", "package_ndc": "70518-3130-2", "marketing_start_date": "20250714"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-3130_3e73d3eb-ffa7-6f9c-e063-6294a90a8666", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-3130", "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": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}