Package 70518-3793-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-3793-0
Digits Only 7051837930
Product NDC 70518-3793
Product ID 70518-3793_43d07619-60fa-01b7-e063-6294a90aeb34
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3793-0)

Marketing

Marketing Status
Marketed Since 2023-07-16
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": "43d07619-60fa-01b7-e063-6294a90aeb34", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["5987a15b-e86f-4fd7-a377-35a917c0e3fe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3793-0)", "package_ndc": "70518-3793-0", "marketing_start_date": "20230716"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "70518-3793_43d07619-60fa-01b7-e063-6294a90aeb34", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3793", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "REMEDYREPACK INC.", "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": "20230716", "listing_expiration_date": "20261231"}