Package 52817-361-00

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 52817-361-00
Digits Only 5281736100
Product NDC 52817-361
Description

1000 TABLET, FILM COATED in 1 BOTTLE (52817-361-00)

Marketing

Marketing Status
Marketed Since 2018-12-01
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": "294dc99d-4a6d-22b6-e063-6394a90a06aa", "openfda": {"upc": ["0352817361103", "0352817361004", "0352817360106", "0352817362100", "0352817358509", "0352817359506", "0352817362001", "0352817360007", "0352817358103", "0352817359100"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924", "1606347", "1606349"], "spl_set_id": ["52c822f2-4a71-4ab2-a470-58074622846a"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (52817-361-00)", "package_ndc": "52817-361-00", "marketing_start_date": "20181201"}, {"sample": true, "description": "100 TABLET, FILM COATED in 1 BOTTLE (52817-361-10)", "package_ndc": "52817-361-10", "marketing_start_date": "20181201"}], "brand_name": "Metoprolol Tartrate", "product_id": "52817-361_294dc99d-4a6d-22b6-e063-6394a90a06aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "52817-361", "generic_name": "Metoprolol Tartrate", "labeler_name": "TruPharma 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": "20181201", "listing_expiration_date": "20261231"}