Package 72162-1293-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1293-1
Digits Only 7216212931
Product NDC 72162-1293
Product ID 72162-1293_a2a413bf-874c-4f93-aaca-a24e27a34696
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1293-1)

Marketing

Marketing Status
Marketed Since 2024-03-11
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": "a2a413bf-874c-4f93-aaca-a24e27a34696", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["d5dbf0d9-9673-4aae-9e28-da9b90bac038"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1293-1)", "package_ndc": "72162-1293-1", "marketing_start_date": "20240311"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72162-1293_a2a413bf-874c-4f93-aaca-a24e27a34696", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72162-1293", "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": "750 mg/1"}], "application_number": "ANDA076756", "marketing_category": "ANDA", "marketing_start_date": "20200806", "listing_expiration_date": "20261231"}