Package 51655-368-52

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-368-52
Digits Only 5165536852
Product NDC 51655-368
Product ID 51655-368_48ebae7a-12c6-3ef3-e063-6294a90a0f21
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-368-52)

Marketing

Marketing Status
Discontinued 2026-11-30
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": "48ebae7a-12c6-3ef3-e063-6294a90a0f21", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["ab80521b-5014-cc2a-e053-2a95a90a2003"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-368-52)", "package_ndc": "51655-368-52", "marketing_end_date": "20261130", "marketing_start_date": "20200604"}], "brand_name": "Metformin Hydrochloride", "product_id": "51655-368_48ebae7a-12c6-3ef3-e063-6294a90a0f21", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "51655-368", "generic_name": "Metformin Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20200604"}