Package 27241-241-90
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
27241-241-90
Digits Only
2724124190
Product NDC
27241-241
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-241-90)
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": "ea6802dc-fb15-47c2-bcff-d7b920ba7986", "openfda": {"upc": ["0327241241901", "0327241240010"], "unii": ["786Z46389E"], "rxcui": ["1807888", "1807915"], "spl_set_id": ["1ed9dde4-339c-486f-a346-dde33a5e493f"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-241-90)", "package_ndc": "27241-241-90", "marketing_start_date": "20210309"}], "brand_name": "Metformin hydrochloride", "product_id": "27241-241_ea6802dc-fb15-47c2-bcff-d7b920ba7986", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "27241-241", "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": "ANDA213962", "marketing_category": "ANDA", "marketing_start_date": "20210309", "listing_expiration_date": "20271231"}