Package 51655-281-25

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package Sample

Package Facts

Identity

Package NDC 51655-281-25
Digits Only 5165528125
Product NDC 51655-281
Product ID 51655-281_48e70fe2-0d8b-38de-e063-6294a90a198d
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-281-25)

Marketing

Marketing Status
Marketed Since 2022-05-11
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": "48e70fe2-0d8b-38de-e063-6294a90a198d", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["e07d2929-7f78-cf63-e053-2995a90af82b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-281-25)", "package_ndc": "51655-281-25", "marketing_start_date": "20220511"}], "brand_name": "Metoprolol Tartrate", "product_id": "51655-281_48e70fe2-0d8b-38de-e063-6294a90a198d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-281", "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": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20220511", "listing_expiration_date": "20271231"}