Package 69367-381-01

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-381-01
Digits Only 6936738101
Product NDC 69367-381
Description

100 TABLET, COATED in 1 BOTTLE (69367-381-01)

Marketing

Marketing Status
Marketed Since 2024-03-04
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": "982c2026-cf0f-449e-9576-2548af623c35", "openfda": {"upc": ["0369367381017", "0369367382014"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["583dac53-65e7-4710-912a-ecd89d07ad03"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (69367-381-01)", "package_ndc": "69367-381-01", "marketing_start_date": "20240304"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (69367-381-05)", "package_ndc": "69367-381-05", "marketing_start_date": "20240304"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (69367-381-10)", "package_ndc": "69367-381-10", "marketing_start_date": "20240304"}], "brand_name": "Metformin Hydrochloride", "product_id": "69367-381_982c2026-cf0f-449e-9576-2548af623c35", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "69367-381", "generic_name": "Metformin Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}