Package 68788-8520-6

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8520-6
Digits Only 6878885206
Product NDC 68788-8520
Product ID 68788-8520_31db7f39-af80-4131-9ef5-96fb74fdd623
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8520-6)

Marketing

Marketing Status
Marketed Since 2023-09-01
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": "31db7f39-af80-4131-9ef5-96fb74fdd623", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807894"], "spl_set_id": ["14238afd-200d-4a05-b731-647c43cecbc3"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8520-6)", "package_ndc": "68788-8520-6", "marketing_start_date": "20230901"}], "brand_name": "Metformin Hydrochloride", "product_id": "68788-8520_31db7f39-af80-4131-9ef5-96fb74fdd623", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68788-8520", "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": "1000 mg/1"}], "application_number": "ANDA090692", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}