Package 70518-3606-2

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-3606-2
Digits Only 7051836062
Product NDC 70518-3606
Product ID 70518-3606_3ac5b360-5e1d-d86f-e063-6394a90a0817
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3606-2)

Marketing

Marketing Status
Marketed Since 2025-02-07
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ac5b360-5e1d-d86f-e063-6394a90a0817", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["18294e2a-62ef-4b74-9649-50d957d88a1d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3606-2)", "package_ndc": "70518-3606-2", "marketing_start_date": "20250207"}], "brand_name": "Metoprolol Tartrate", "product_id": "70518-3606_3ac5b360-5e1d-d86f-e063-6394a90a0817", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3606", "generic_name": "Metoprolol Tartrate", "labeler_name": "REMEDYREPACK 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": "20230104", "listing_expiration_date": "20261231"}