Package 68645-478-54

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 68645-478-54
Digits Only 6864547854
Product NDC 68645-478
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-478-54)

Marketing

Marketing Status
Marketed Since 2012-09-10
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": "9732391a-6668-4cbe-96ac-575496e378e0", "openfda": {"upc": ["0368645478548", "0368645477541"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["98d31d43-eff0-4ba9-9953-f2f53c13b3d9"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-478-54)", "package_ndc": "68645-478-54", "marketing_start_date": "20120910"}], "brand_name": "Metoprolol succinate", "product_id": "68645-478_9732391a-6668-4cbe-96ac-575496e378e0", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68645-478", "generic_name": "Metoprolol succinate", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20120910", "listing_expiration_date": "20271231"}