Package 82009-114-05

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 82009-114-05
Digits Only 8200911405
Product NDC 82009-114
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-114-05)

Marketing

Marketing Status
Marketed Since 2023-07-20
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": "5d95a380-8fd1-df65-473b-277cb1c064d4", "openfda": {"upc": ["0382009113050", "0382009114057"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["250c2428-c8b0-5156-697a-60cb8a45713c"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-114-05)", "package_ndc": "82009-114-05", "marketing_start_date": "20230720"}], "brand_name": "Metoprolol succinate", "product_id": "82009-114_5d95a380-8fd1-df65-473b-277cb1c064d4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82009-114", "generic_name": "Metoprolol succinate", "labeler_name": "Quallent Pharmaceuticals Health 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": "20230720", "listing_expiration_date": "20261231"}