Package 70010-497-09
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
70010-497-09
Digits Only
7001049709
Product NDC
70010-497
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-497-09)
Marketing
Marketing Status
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": "1c56aa5b-703f-fa8d-e063-6394a90abcb2", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807888", "1807915"], "spl_set_id": ["a5980bc8-8de8-c456-e053-2a95a90a792e"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-497-09)", "package_ndc": "70010-497-09", "marketing_start_date": "20210122"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "70010-497_1c56aa5b-703f-fa8d-e063-6394a90abcb2", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70010-497", "generic_name": "Metformin Hydrochloride", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA213344", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}