Package 72189-659-90
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
72189-659-90
Digits Only
7218965990
Product NDC
72189-659
Description
90 TABLET in 1 BOTTLE (72189-659-90)
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": "499ce022-12a8-e4e5-e063-6394a90a435a", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["499ce022-12a7-e4e5-e063-6394a90a435a"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-659-90)", "package_ndc": "72189-659-90", "marketing_start_date": "20260130"}], "brand_name": "Metoprolol Tartrate", "product_id": "72189-659_499ce022-12a8-e4e5-e063-6394a90a435a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-659", "generic_name": "Metoprolol Tartrate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20260130", "listing_expiration_date": "20271231"}