Package 82009-116-05

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 82009-116-05
Digits Only 8200911605
Product NDC 82009-116
Product ID 82009-116_65151fb6-9d77-fb5b-bde1-8d78322e4a1a
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-116-05)

Marketing

Marketing Status
Marketed Since 2023-07-20
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": "65151fb6-9d77-fb5b-bde1-8d78322e4a1a", "openfda": {"upc": ["0382009116051", "0382009115054"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419"], "spl_set_id": ["e147a897-4a23-1e1a-73cd-f2e6c9a7280d"], "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 (82009-116-05)", "package_ndc": "82009-116-05", "marketing_start_date": "20230720"}], "brand_name": "Metoprolol succinate", "product_id": "82009-116_65151fb6-9d77-fb5b-bde1-8d78322e4a1a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82009-116", "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": "200 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20230720", "listing_expiration_date": "20261231"}