Package 51655-203-52

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 51655-203-52
Digits Only 5165520352
Product NDC 51655-203
Product ID 51655-203_48d28f1e-85e7-e178-e063-6394a90af983
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-203-52)

Marketing

Marketing Status
Marketed Since 2020-09-01
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Metoprolol Succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48d28f1e-85e7-e178-e063-6394a90af983", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["c213c327-68b7-da5b-e053-2a95a90a4028"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-203-52)", "package_ndc": "51655-203-52", "marketing_start_date": "20200901"}], "brand_name": "Metoprolol Succinate", "product_id": "51655-203_48d28f1e-85e7-e178-e063-6394a90af983", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-203", "generic_name": "Metoprolol succinate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204106", "marketing_category": "ANDA", "marketing_start_date": "20200901", "listing_expiration_date": "20271231"}