Package 72162-1522-5

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1522-5
Digits Only 7216215225
Product NDC 72162-1522
Description

500 TABLET in 1 BOTTLE (72162-1522-5)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": "46e0a696-b726-4315-8b2d-04c4a6deae29", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["f9e78e0f-6a0a-4db3-bc09-5500748f9c84"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1522-1)", "package_ndc": "72162-1522-1", "marketing_start_date": "20240205"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1522-5)", "package_ndc": "72162-1522-5", "marketing_start_date": "20240205"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72162-1522_46e0a696-b726-4315-8b2d-04c4a6deae29", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72162-1522", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}