Package 17224-311-28
Brand: metformin hydrochloride extended-release 500mg
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
17224-311-28
Digits Only
1722431128
Product NDC
17224-311
Description
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-311-28)
Marketing
Marketing Status
Brand
metformin hydrochloride extended-release 500mg
Generic
metformin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "da8083b6-aeff-e1ee-e053-2a95a90a0844", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["e9cd0d23-56eb-40dd-abf4-9e681ec220f5"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-311-28)", "package_ndc": "17224-311-28", "marketing_start_date": "20170608"}], "brand_name": "Metformin Hydrochloride Extended-Release 500mg", "product_id": "17224-311_da8083b6-aeff-e1ee-e053-2a95a90a0844", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "17224-311", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride Extended-Release 500mg", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20170608", "listing_expiration_date": "20261231"}