Package 50090-7878-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7878-0
Digits Only 5009078780
Product NDC 50090-7878
Product ID 50090-7878_ed142b0d-07ed-436a-9fbf-af1b31d6c615
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7878-0)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "ed142b0d-07ed-436a-9fbf-af1b31d6c615", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["5f2023d2-05ae-489d-9e18-fb75057496bc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7878-0)", "package_ndc": "50090-7878-0", "marketing_start_date": "20260202"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7878_ed142b0d-07ed-436a-9fbf-af1b31d6c615", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7878", "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": "1000 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20250825", "listing_expiration_date": "20271231"}