Package 67457-251-02

Brand: dexmedetomidine

Generic: dexmedetomidine
NDC Package

Package Facts

Identity

Package NDC 67457-251-02
Digits Only 6745725102
Product NDC 67457-251
Description

25 VIAL, GLASS in 1 CARTON (67457-251-02) / 2 mL in 1 VIAL, GLASS (67457-251-00)

Marketing

Marketing Status
Marketed Since 2014-08-18
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": "7c66a6ac-0548-4555-b9d1-077feb277c37", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["ebdfe2e8-30ca-4f18-935a-41bcbbce4937"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (67457-251-02)  / 2 mL in 1 VIAL, GLASS (67457-251-00)", "package_ndc": "67457-251-02", "marketing_start_date": "20140818"}], "brand_name": "Dexmedetomidine", "product_id": "67457-251_7c66a6ac-0548-4555-b9d1-077feb277c37", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "67457-251", "generic_name": "dexmedetomidine", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA202881", "marketing_category": "ANDA", "marketing_start_date": "20140818", "listing_expiration_date": "20261231"}