NDC 0409-0155

Precedex

Dexmedetomidine Hydrochloride

Precedex is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Dexmedetomidine Hydrochloride.

• Product ID: 0409-0155_6022b926-e30f-4d6f-902b-5974e77d3152
• NDC: 0409-0155
• Product Type: Human Prescription Drug
• Proprietary Name: Precedex
• Generic Name: Dexmedetomidine Hydrochloride
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2023-01-03
• Marketing Category: NDA /
• Application Number: NDA021038
• Labeler Name: Hospira, Inc.
• Substance Name: DEXMEDETOMIDINE HYDROCHLORIDE
• Active Ingredient Strength: 4 ug/mL
• Pharm Classes: Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2024-12-31

Packaging

NDC 0409-0155-02

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

• Marketing Start Date: 2023-01-03
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Precedex" or generic name "Dexmedetomidine Hydrochloride"

NDC	Brand Name	Generic Name
0404-9938	PRECEDEX	DEXMEDETOMIDINE HYDROCHLORIDE
0409-0155	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
0409-1174	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
0409-1434	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
0409-1454	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
0409-1638	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
0409-1660	Precedex	DEXMEDETOMIDINE HYDROCHLORIDE
52584-638	PRECEDEX	PRECEDEX
0143-9525	Dexmedetomidine Hydrochloride	Dexmedetomidine Hydrochloride
0143-9526	Dexmedetomidine Hydrochloride	Dexmedetomidine Hydrochloride
0338-9555	DEXMEDETOMIDINE HYDROCHLORIDE	DEXMEDETOMIDINE HYDROCHLORIDE
0338-9557	DEXMEDETOMIDINE HYDROCHLORIDE	DEXMEDETOMIDINE HYDROCHLORIDE