Package 71610-837-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-837-60
Digits Only 7161083760
Product NDC 71610-837
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-60)

Marketing

Marketing Status
Marketed Since 2024-05-31
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": "1a0499c1-6f4c-d51b-e063-6294a90a72fb", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["1a047fc0-196e-79af-e063-6394a90a1e0d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-30)", "package_ndc": "71610-837-30", "marketing_start_date": "20240531"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-53)", "package_ndc": "71610-837-53", "marketing_start_date": "20240531"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-60)", "package_ndc": "71610-837-60", "marketing_start_date": "20240531"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-70)", "package_ndc": "71610-837-70", "marketing_start_date": "20240531"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-80)", "package_ndc": "71610-837-80", "marketing_start_date": "20240531"}, {"sample": false, "description": "360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-94)", "package_ndc": "71610-837-94", "marketing_start_date": "20240531"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "71610-837_1a0499c1-6f4c-d51b-e063-6294a90a72fb", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71610-837", "generic_name": "metformin hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA201991", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}