Package 27241-189-60
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
27241-189-60
Digits Only
2724118960
Product NDC
27241-189
Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-189-60)
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": "694fc444-2414-4d97-8fe5-53bb6d85ee5d", "openfda": {"upc": ["0327241189609", "0327241188602"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["6d9179a8-9579-4804-a4c7-633f37aef1ee"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-189-60)", "package_ndc": "27241-189-60", "marketing_start_date": "20200409"}], "brand_name": "Metformin hydrochloride", "product_id": "27241-189_694fc444-2414-4d97-8fe5-53bb6d85ee5d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "27241-189", "generic_name": "Metformin hydrochloride", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA213651", "marketing_category": "ANDA", "marketing_start_date": "20200409", "listing_expiration_date": "20271231"}