Package 82804-195-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-195-60
Digits Only 8280419560
Product NDC 82804-195
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-195-60)

Marketing

Marketing Status
Marketed Since 2025-02-10
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": "7cb47c3e-6657-4c11-8aa2-ae172e5a8529", "openfda": {"upc": ["0382804195602"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["7cb47c3e-6657-4c11-8aa2-ae172e5a8529"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-195-60)", "package_ndc": "82804-195-60", "marketing_start_date": "20250210"}], "brand_name": "Metformin Hydrochloride", "product_id": "82804-195_7cb47c3e-6657-4c11-8aa2-ae172e5a8529", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82804-195", "generic_name": "Metformin Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}