Package 55150-209-02

Brand: dexmedetomidine

Generic: dexmedetomidine
NDC Package

Package Facts

Identity

Package NDC 55150-209-02
Digits Only 5515020902
Product NDC 55150-209
Description

25 VIAL in 1 CARTON (55150-209-02) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2016-03-17
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": "72d6b6e6-236e-44f8-a747-de2ee97bca87", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710", "1718906", "1718909"], "spl_set_id": ["8c162541-986b-4b30-866c-b2631ba2c975"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (55150-209-02)  / 2 mL in 1 VIAL", "package_ndc": "55150-209-02", "marketing_start_date": "20160317"}], "brand_name": "Dexmedetomidine", "product_id": "55150-209_72d6b6e6-236e-44f8-a747-de2ee97bca87", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "55150-209", "generic_name": "Dexmedetomidine", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA205867", "marketing_category": "ANDA", "marketing_start_date": "20160317", "listing_expiration_date": "20261231"}