Package 50090-5052-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5052-0
Digits Only 5009050520
Product NDC 50090-5052
Product ID 50090-5052_c8113533-5e20-4b42-9a2a-b634f32c780c
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-5052-0)

Marketing

Marketing Status
Marketed Since 2020-05-19
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": "c8113533-5e20-4b42-9a2a-b634f32c780c", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["afb183f6-a13c-4f00-82d5-9fe336173d34"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5052-0)", "package_ndc": "50090-5052-0", "marketing_start_date": "20200519"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-5052_c8113533-5e20-4b42-9a2a-b634f32c780c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-5052", "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": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20050114", "listing_expiration_date": "20261231"}