Package 42291-497-10
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
42291-497-10
Digits Only
4229149710
Product NDC
42291-497
Description
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-497-10)
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": "485f88a3-e04c-a929-e063-6394a90a524d", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["db4a1415-6d46-15bb-e053-2a95a90a3c97"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-497-10)", "package_ndc": "42291-497-10", "marketing_start_date": "20220328"}], "brand_name": "Metformin Hydrochloride", "product_id": "42291-497_485f88a3-e04c-a929-e063-6394a90a524d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "42291-497", "generic_name": "Metformin Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078596", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20271231"}