Package 42806-405-60
Brand: metformin hydrochloride
Generic: metformin hydrochloride tabletsPackage Facts
Identity
Package NDC
42806-405-60
Digits Only
4280640560
Product NDC
42806-405
Description
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-405-60)
Marketing
Marketing Status
Brand
metformin hydrochloride
Generic
metformin hydrochloride tablets
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1edb3813-b7cb-4501-ad91-eae58624c836", "openfda": {"upc": ["0342806406601", "0342806405604"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["356b02d0-d239-4441-bb33-c4c54166fcd7"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-405-60)", "package_ndc": "42806-405-60", "marketing_start_date": "20190104"}], "brand_name": "metformin hydrochloride", "product_id": "42806-405_1edb3813-b7cb-4501-ad91-eae58624c836", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "42806-405", "generic_name": "metformin hydrochloride tablets", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209993", "marketing_category": "ANDA", "marketing_start_date": "20190104", "listing_expiration_date": "20271231"}