Package 27241-241-90

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package 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
Marketed Since 2021-03-09
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"}