Package 0409-2815-01

Brand: precedex

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-2815-01
Digits Only 0409281501
Product NDC 0409-2815
Description

1 BOTTLE in 1 CARTON (0409-2815-01) / 250 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-01-17
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": "8d48de06-361f-418b-bfec-8ef85f94d5bc", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718900", "1718902", "1718906", "1718907", "1718909", "1718910", "2396891", "2396892"], "spl_set_id": ["4419162d-81d4-49bd-96de-1729440bdb74"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0409-2815-01)  / 250 mL in 1 BOTTLE", "package_ndc": "0409-2815-01", "marketing_start_date": "20230117"}], "brand_name": "Precedex", "product_id": "0409-2815_8d48de06-361f-418b-bfec-8ef85f94d5bc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "0409-2815", "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": "20230117", "listing_expiration_date": "20261231"}