Package 72789-400-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-400-60
Digits Only 7278940060
Product NDC 72789-400
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-60)

Marketing

Marketing Status
Marketed Since 2024-06-03
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": "3cf82ef5-5b60-2c45-e063-6394a90a5d62", "openfda": {"upc": ["0372789400600"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["9171d369-d35a-40e4-a9ad-26484e66fc5e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-01)", "package_ndc": "72789-400-01", "marketing_start_date": "20250115"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-60)", "package_ndc": "72789-400-60", "marketing_start_date": "20240603"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-82)", "package_ndc": "72789-400-82", "marketing_start_date": "20240603"}, {"sample": false, "description": "360 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-86)", "package_ndc": "72789-400-86", "marketing_start_date": "20240517"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-90)", "package_ndc": "72789-400-90", "marketing_start_date": "20240517"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-400-93)", "package_ndc": "72789-400-93", "marketing_start_date": "20240517"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72789-400_3cf82ef5-5b60-2c45-e063-6394a90a5d62", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-400", "generic_name": "metformin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA201991", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}