Package 72789-409-90

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-409-90
Digits Only 7278940990
Product NDC 72789-409
Product ID 72789-409_48334c7e-36f3-00ff-e063-6394a90a3f42
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90)

Marketing

Marketing Status
Discontinued 2027-03-31
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": "48334c7e-36f3-00ff-e063-6394a90a3f42", "openfda": {"upc": ["0372789409900"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["e3e9b582-fd15-4fe0-a210-398d9149696e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90)", "package_ndc": "72789-409-90", "marketing_end_date": "20270331", "marketing_start_date": "20240607"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72789-409_48334c7e-36f3-00ff-e063-6394a90a3f42", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-409", "generic_name": "metformin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20230119"}