Package 0409-0155-02

Brand: precedex

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-0155-02
Digits Only 0409015502
Product NDC 0409-0155
Description

10 BOTTLE in 1 TRAY (0409-0155-02) / 100 mL in 1 BOTTLE (0409-0155-01)

Marketing

Marketing Status
Marketed Since 2023-01-03
Brand precedex
Generic dexmedetomidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1fdb4815-2990-4926-ba76-25241810489e", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718907", "1718909", "1718910"], "spl_set_id": ["92b7ddaa-e45a-4b64-a802-bb5df8771dd6"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BOTTLE in 1 TRAY (0409-0155-02)  / 100 mL in 1 BOTTLE (0409-0155-01)", "package_ndc": "0409-0155-02", "marketing_start_date": "20230103"}], "brand_name": "Precedex", "product_id": "0409-0155_1fdb4815-2990-4926-ba76-25241810489e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "0409-0155", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Precedex", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "NDA021038", "marketing_category": "NDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}