Package 66689-318-16

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66689-318-16
Digits Only 6668931816
Product NDC 66689-318
Description

1 BOTTLE in 1 CARTON (66689-318-16) / 473 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-12-19
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": "88a5077b-b1b5-47bb-ab45-32de55907ea6", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861025"], "spl_set_id": ["e087ce3b-8d7f-43a3-8d20-54513da7617d"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (66689-318-16)  / 473 mL in 1 BOTTLE", "package_ndc": "66689-318-16", "marketing_start_date": "20221219"}], "brand_name": "Metformin Hydrochloride", "product_id": "66689-318_88a5077b-b1b5-47bb-ab45-32de55907ea6", "dosage_form": "SOLUTION", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "66689-318", "generic_name": "Metformin Hydrochloride", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/5mL"}], "application_number": "ANDA212677", "marketing_category": "ANDA", "marketing_start_date": "20221219", "listing_expiration_date": "20261231"}