Package 72603-143-01

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 72603-143-01
Digits Only 7260314301
Product NDC 72603-143
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01)

Marketing

Marketing Status
Marketed Since 2023-04-10
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": "82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3", "openfda": {"upc": ["0372603143010", "0372603142013"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["ad097646-cc77-8d67-5974-cc00060409f2"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01)", "package_ndc": "72603-143-01", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-02)", "package_ndc": "72603-143-02", "marketing_start_date": "20230410"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)", "package_ndc": "72603-143-03", "marketing_start_date": "20230912"}], "brand_name": "Metoprolol succinate", "product_id": "72603-143_82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-143", "generic_name": "Metoprolol succinate", "labeler_name": "Northstar Rx 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": "20230410", "listing_expiration_date": "20261231"}