Package 72789-455-30

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-455-30
Digits Only 7278945530
Product NDC 72789-455
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-455-30)

Marketing

Marketing Status
Marketed Since 2024-12-05
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": "3cf839a3-34a6-736c-e063-6394a90a8ae5", "openfda": {"upc": ["0372789455303"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["f55a245b-a786-4a4a-b11c-c61d48294b01"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-455-30)", "package_ndc": "72789-455-30", "marketing_start_date": "20241205"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72789-455_3cf839a3-34a6-736c-e063-6394a90a8ae5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-455", "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"}