Package 70518-2615-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-2615-0
Digits Only 7051826150
Product NDC 70518-2615
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2615-0)

Marketing

Marketing Status
Marketed Since 2020-03-09
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a7a3dc5-5297-5bed-e063-6294a90a2d82", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["028b6e4a-1597-4d21-89d0-0bbbad21efa8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2615-0)", "package_ndc": "70518-2615-0", "marketing_start_date": "20200309"}], "brand_name": "Metoprolol Tartrate", "product_id": "70518-2615_4a7a3dc5-5297-5bed-e063-6294a90a2d82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-2615", "generic_name": "Metoprolol Tartrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20200309", "listing_expiration_date": "20271231"}