dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloride
Labeler: baxter healthcare companyDrug Facts
Product Profile
Brand Name
dexmedetomidine hydrochloride
Generic Name
dexmedetomidine hydrochloride
Labeler
baxter healthcare company
Dosage Form
INJECTION
Routes
Active Ingredients
dexmedetomidine hydrochloride 200 ug/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-9555
Product ID
0338-9555_594e9faa-bc32-42e0-9c0a-8fa9460b1e24
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208532
Listing Expiration
2027-12-31
Marketing Start
2018-08-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03389555
Hyphenated Format
0338-9555
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
dexmedetomidine hydrochloride (source: ndc)
Generic Name
dexmedetomidine hydrochloride (source: ndc)
Application Number
ANDA208532 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 ug/50mL
Packaging
- 24 BAG in 1 CARTON (0338-9555-24) / 50 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "594e9faa-bc32-42e0-9c0a-8fa9460b1e24", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["8ccb45a7-8290-469c-9644-a4dca967d88f"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-9555-24) / 50 mL in 1 BAG", "package_ndc": "0338-9555-24", "marketing_start_date": "20180821"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "product_id": "0338-9555_594e9faa-bc32-42e0-9c0a-8fa9460b1e24", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "0338-9555", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "200 ug/50mL"}], "application_number": "ANDA208532", "marketing_category": "ANDA", "marketing_start_date": "20180821", "listing_expiration_date": "20271231"}