Package 70518-2080-1

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 70518-2080-1
Digits Only 7051820801
Product NDC 70518-2080
Product ID 70518-2080_388fcc07-60b9-bfe5-e063-6394a90ad22f
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2080-1)

Marketing

Marketing Status
Marketed Since 2023-01-19
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Metoprolol succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "388fcc07-60b9-bfe5-e063-6394a90ad22f", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["35304060-0965-488d-9e6e-bd1217286ea1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2080-1)", "package_ndc": "70518-2080-1", "marketing_start_date": "20230119"}], "brand_name": "Metoprolol succinate", "product_id": "70518-2080_388fcc07-60b9-bfe5-e063-6394a90ad22f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-2080", "generic_name": "Metoprolol succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20190514", "listing_expiration_date": "20261231"}