Package 51655-884-52

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package Sample

Package Facts

Identity

Package NDC 51655-884-52
Digits Only 5165588452
Product NDC 51655-884
Product ID 51655-884_4973fd67-4cd3-1b98-e063-6394a90a103b
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-884-52)

Marketing

Marketing Status
Marketed Since 2022-03-02
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package Yes

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4973fd67-4cd3-1b98-e063-6394a90a103b", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["d9df7d01-339c-8985-e053-2a95a90a0d2c"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-884-52)", "package_ndc": "51655-884-52", "marketing_start_date": "20220302"}], "brand_name": "Metoprolol Tartrate", "product_id": "51655-884_4973fd67-4cd3-1b98-e063-6394a90a103b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-884", "generic_name": "Metoprolol Tartrate", "labeler_name": "Northwind Health Company, LLC", "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": "20220302", "listing_expiration_date": "20271231"}