Package 45963-678-11

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 45963-678-11
Digits Only 4596367811
Product NDC 45963-678
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-678-11)

Marketing

Marketing Status
Marketed Since 2019-10-23
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e51ef0b9-fe4a-473c-92a0-6043fdb0b620", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["b798601e-a369-4c8b-8235-08900e1b751d"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-678-11)", "package_ndc": "45963-678-11", "marketing_start_date": "20191023"}], "brand_name": "metoprolol succinate", "product_id": "45963-678_e51ef0b9-fe4a-473c-92a0-6043fdb0b620", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "45963-678", "generic_name": "metoprolol succinate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "200 mg/1"}], "application_number": "ANDA204161", "marketing_category": "ANDA", "marketing_start_date": "20191023", "listing_expiration_date": "20261231"}