Package 51662-1365-1

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 51662-1365-1
Digits Only 5166213651
Product NDC 51662-1365
Description

5 mL in 1 VIAL (51662-1365-1)

Marketing

Marketing Status
Marketed Since 2019-12-08
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef7bd5a0-02a7-7b66-e053-2995a90a8ffa", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866508"], "spl_set_id": ["993c3a0d-5472-3de3-e053-2995a90acdf6"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL (51662-1365-1)", "package_ndc": "51662-1365-1", "marketing_start_date": "20191208"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "51662-1365_ef7bd5a0-02a7-7b66-e053-2995a90a8ffa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1365", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "5 mg/5mL"}], "application_number": "ANDA091045", "marketing_category": "ANDA", "marketing_start_date": "20191208", "listing_expiration_date": "20261231"}