Package 50268-550-15

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-550-15
Digits Only 5026855015
Product NDC 50268-550
Description

50 BLISTER PACK in 1 BOX (50268-550-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-550-11)

Marketing

Marketing Status
Marketed Since 2022-03-08
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": "47e74e26-3f97-482a-e063-6394a90a3ac9", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["d9bac244-1725-5bf3-e053-2a95a90ac823"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-550-15)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-550-11)", "package_ndc": "50268-550-15", "marketing_start_date": "20220308"}], "brand_name": "Metformin Hydrochloride", "product_id": "50268-550_47e74e26-3f97-482a-e063-6394a90a3ac9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50268-550", "generic_name": "Metformin Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20220308", "listing_expiration_date": "20271231"}