Package 50090-6859-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6859-0
Digits Only 5009068590
Product NDC 50090-6859
Product ID 50090-6859_90eb2489-645a-4863-a95c-53a1b3389f2c
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6859-0)

Marketing

Marketing Status
Marketed Since 2023-12-01
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": "90eb2489-645a-4863-a95c-53a1b3389f2c", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["192970d3-826a-4b69-a525-9742794dc19c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6859-0)", "package_ndc": "50090-6859-0", "marketing_start_date": "20231201"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-6859_90eb2489-645a-4863-a95c-53a1b3389f2c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-6859", "generic_name": "Metformin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20210517", "listing_expiration_date": "20271231"}