Package 51655-649-52

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-649-52
Digits Only 5165564952
Product NDC 51655-649
Product ID 51655-649_494f8087-f75c-8014-e063-6294a90ac94c
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)

Marketing

Marketing Status
Marketed Since 2021-04-01
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": "494f8087-f75c-8014-e063-6294a90ac94c", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["db113f46-6fac-9005-e053-2995a90a017a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)", "package_ndc": "51655-649-26", "marketing_start_date": "20230623"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)", "package_ndc": "51655-649-52", "marketing_start_date": "20210401"}], "brand_name": "Metformin Hydrochloride", "product_id": "51655-649_494f8087-f75c-8014-e063-6294a90ac94c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "51655-649", "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": "1000 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}