Package 30698-459-01

Brand: lopressor

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 30698-459-01
Digits Only 3069845901
Product NDC 30698-459
Description

100 TABLET in 1 BOTTLE (30698-459-01)

Marketing

Marketing Status
Marketed Since 2014-05-05
Brand lopressor
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28c4fc69-5609-49ec-8fe5-4d7bc8f88288", "openfda": {"upc": ["0330698459010"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866513", "866514", "866516"], "spl_set_id": ["0283bc9d-6998-493a-824a-d4c85f704111"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-459-01)", "package_ndc": "30698-459-01", "marketing_start_date": "20140505"}], "brand_name": "Lopressor", "product_id": "30698-459_28c4fc69-5609-49ec-8fe5-4d7bc8f88288", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "30698-459", "generic_name": "metoprolol tartrate", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lopressor", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "NDA017963", "marketing_category": "NDA", "marketing_start_date": "20140505", "listing_expiration_date": "20261231"}