Package 71872-7323-1

Brand: dexmedetomidine

Generic: dexmedetomidine
NDC Package

Package Facts

Identity

Package NDC 71872-7323-1
Digits Only 7187273231
Product NDC 71872-7323
Description

1 VIAL, GLASS in 1 BAG (71872-7323-1) / 2 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2024-01-22
Brand dexmedetomidine
Generic dexmedetomidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "12ef0602-bf08-6ddd-e063-6294a90a23c3", "openfda": {"upc": ["0371872732314"], "unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["12ef0602-bf07-6ddd-e063-6294a90a23c3"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 BAG (71872-7323-1)  / 2 mL in 1 VIAL, GLASS", "package_ndc": "71872-7323-1", "marketing_start_date": "20240122"}], "brand_name": "Dexmedetomidine", "product_id": "71872-7323_12ef0602-bf08-6ddd-e063-6294a90a23c3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71872-7323", "generic_name": "Dexmedetomidine", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "200 ug/2mL"}], "application_number": "ANDA202126", "marketing_category": "ANDA", "marketing_start_date": "20210119", "listing_expiration_date": "20261231"}