Package 72603-144-03

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 72603-144-03
Digits Only 7260314403
Product NDC 72603-144
Description

1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-03)

Marketing

Marketing Status
Marketed Since 2023-09-12
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": "ab3584df-a821-6eb3-7548-0306ce2d1a8a", "openfda": {"upc": ["0372603144017", "0372603145014"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419"], "spl_set_id": ["d887be8a-e6c2-5129-edbd-d7b2c0283dca"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-01)", "package_ndc": "72603-144-01", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-02)", "package_ndc": "72603-144-02", "marketing_start_date": "20230410"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-144-03)", "package_ndc": "72603-144-03", "marketing_start_date": "20230912"}], "brand_name": "Metoprolol succinate", "product_id": "72603-144_ab3584df-a821-6eb3-7548-0306ce2d1a8a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-144", "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": "100 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}