Package 59651-043-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-043-60
Digits Only 5965104360
Product NDC 59651-043
Product ID 59651-043_ef77c7dd-a65f-4adc-a0d9-a93779b459a0
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-043-60)

Marketing

Marketing Status
Marketed Since 2024-10-18
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": "ef77c7dd-a65f-4adc-a0d9-a93779b459a0", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["ef77c7dd-a65f-4adc-a0d9-a93779b459a0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-043-60)", "package_ndc": "59651-043-60", "marketing_start_date": "20241018"}], "brand_name": "Metformin Hydrochloride", "product_id": "59651-043_ef77c7dd-a65f-4adc-a0d9-a93779b459a0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "59651-043", "generic_name": "Metformin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209694", "marketing_category": "ANDA", "marketing_start_date": "20241018", "listing_expiration_date": "20261231"}