Package 0404-9938-02

Brand: precedex

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9938-02
Digits Only 0404993802
Product NDC 0404-9938
Description

1 VIAL in 1 BAG (0404-9938-02) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-13
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": "a852ab49-191f-4755-8035-a2979d8b6489", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["284397", "309710"], "spl_set_id": ["9eb336de-5fa5-4b46-b40b-a7ca5a0864bd"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9938-02)  / 2 mL in 1 VIAL", "package_ndc": "0404-9938-02", "marketing_start_date": "20220113"}], "brand_name": "PRECEDEX", "product_id": "0404-9938_a852ab49-191f-4755-8035-a2979d8b6489", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "0404-9938", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRECEDEX", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "NDA021038", "marketing_category": "NDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}