precedex
Generic: dexmedetomidine hydrochloride
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
precedex
Generic Name
dexmedetomidine hydrochloride
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dexmedetomidine hydrochloride 4 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-4596
Product ID
0409-4596_1fdb4815-2990-4926-ba76-25241810489e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021038
Listing Expiration
2026-12-31
Marketing Start
2023-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094596
Hyphenated Format
0409-4596
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
precedex (source: ndc)
Generic Name
dexmedetomidine hydrochloride (source: ndc)
Application Number
NDA021038 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 ug/mL
Packaging
- 20 BOTTLE in 1 TRAY (0409-4596-20) / 50 mL in 1 BOTTLE (0409-4596-01)
Packages (1)
Ingredients (1)
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": "20 BOTTLE in 1 TRAY (0409-4596-20) / 50 mL in 1 BOTTLE (0409-4596-01)", "package_ndc": "0409-4596-20", "marketing_start_date": "20230103"}], "brand_name": "Precedex", "product_id": "0409-4596_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": "0409-4596", "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"}