Package 68788-8564-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8564-1
Digits Only 6878885641
Product NDC 68788-8564
Product ID 68788-8564_d05d2f97-e42b-43f7-a89d-820224a6822e
Description

100 TABLET in 1 BOTTLE (68788-8564-1)

Marketing

Marketing Status
Discontinued 2026-09-30
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": "d05d2f97-e42b-43f7-a89d-820224a6822e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["5073c482-952c-400c-afff-64380f133bc8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8564-1)", "package_ndc": "68788-8564-1", "marketing_end_date": "20260930", "marketing_start_date": "20240111"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68788-8564_d05d2f97-e42b-43f7-a89d-820224a6822e", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68788-8564", "generic_name": "metformin hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20240111"}