Package 72789-549-93
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
72789-549-93
Digits Only
7278954993
Product NDC
72789-549
Description
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-549-93)
Marketing
Marketing Status
Brand
metoprolol tartrate
Generic
metoprolol tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4883e502-4d3d-8341-e063-6294a90a3077", "openfda": {"upc": ["0372789549934"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["18f44ba2-d431-4a73-ac78-83e734fde694"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-549-93)", "package_ndc": "72789-549-93", "marketing_start_date": "20260116"}], "brand_name": "Metoprolol Tartrate", "product_id": "72789-549_4883e502-4d3d-8341-e063-6294a90a3077", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-549", "generic_name": "Metoprolol Tartrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20271231"}