Package 59651-758-01
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
59651-758-01
Digits Only
5965175801
Product NDC
59651-758
Description
100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)
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": "2d3b41ae-f657-4459-bdee-e76e644ec167", "openfda": {"upc": ["0359651760017", "0359651758014"], "unii": ["W5S57Y3A5L"], "rxcui": ["1606347", "1606349"], "spl_set_id": ["ac4ac150-d3e6-4bd1-8a4a-7d63fade3e49"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)", "package_ndc": "59651-758-01", "marketing_start_date": "20231207"}], "brand_name": "Metoprolol Tartrate", "product_id": "59651-758_2d3b41ae-f657-4459-bdee-e76e644ec167", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-758", "generic_name": "Metoprolol Tartrate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "37.5 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20231207", "listing_expiration_date": "20261231"}