Package 67296-1701-6

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1701-6
Digits Only 6729617016
Product NDC 67296-1701
Product ID 67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)

Marketing

Marketing Status
Marketed Since 2019-11-01
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": "2c62e72c-7dec-d183-e063-6394a90a9d2b", "openfda": {"upc": ["0367296170139"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["fc61bafa-a506-14ae-e053-6394a90a9c7d"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)", "package_ndc": "67296-1701-6", "marketing_start_date": "20191101"}], "brand_name": "Metformin Hydrochloride", "product_id": "67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67296-1701", "generic_name": "Metformin Hydrochloride", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}