Package 67046-1569-3

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 67046-1569-3
Digits Only 6704615693
Product NDC 67046-1569
Description

30 TABLET in 1 BLISTER PACK (67046-1569-3)

Marketing

Marketing Status
Marketed Since 2025-06-17
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": "37c9bb2e-5706-18e7-e063-6394a90a9ccf", "openfda": {"upc": ["0352817252005"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["37c9c12a-db53-1fd6-e063-6394a90afb92"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1569-3)", "package_ndc": "67046-1569-3", "marketing_start_date": "20250617"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "67046-1569_37c9bb2e-5706-18e7-e063-6394a90a9ccf", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67046-1569", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}