Package 70518-3997-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-3997-0
Digits Only 7051839970
Product NDC 70518-3997
Description

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3997-0)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "3d43c168-92bc-fcdd-e063-6294a90a2e96", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["ad7a07a1-a05f-4eee-ba0a-69675ffbb6e8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3997-0)", "package_ndc": "70518-3997-0", "marketing_start_date": "20240126"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3997-1)", "package_ndc": "70518-3997-1", "marketing_start_date": "20250730"}], "brand_name": "Metoprolol Tartrate", "product_id": "70518-3997_3d43c168-92bc-fcdd-e063-6294a90a2e96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3997", "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": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20240126", "listing_expiration_date": "20261231"}