Package 82009-180-05

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-180-05
Digits Only 8200918005
Product NDC 82009-180
Product ID 82009-180_29ba0029-582f-4f13-9f1c-c47b5b9ccdb0
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-180-05)

Marketing

Marketing Status
Marketed Since 2025-12-15
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": "29ba0029-582f-4f13-9f1c-c47b5b9ccdb0", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["6864ff5a-7512-4a4f-ad26-b2b9c5843414"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-180-05)", "package_ndc": "82009-180-05", "marketing_start_date": "20251215"}], "brand_name": "Metformin Hydrochloride", "product_id": "82009-180_29ba0029-582f-4f13-9f1c-c47b5b9ccdb0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82009-180", "generic_name": "Metformin Hydrochloride", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA206145", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20271231"}