Package 42023-146-25
Brand: dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloridePackage Facts
Identity
Package NDC
42023-146-25
Digits Only
4202314625
Product NDC
42023-146
Description
25 VIAL in 1 CARTON (42023-146-25) / 2 mL in 1 VIAL
Marketing
Marketing Status
Brand
dexmedetomidine hydrochloride
Generic
dexmedetomidine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a8946a56-56ee-4169-8fec-1c8fffaf9642", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710", "1718906", "1718909"], "spl_set_id": ["1ee59985-4c1d-48f7-b8f9-5584c2d55e08"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (42023-146-25) / 2 mL in 1 VIAL", "package_ndc": "42023-146-25", "marketing_start_date": "20140819"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "42023-146_a8946a56-56ee-4169-8fec-1c8fffaf9642", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "42023-146", "generic_name": "Dexmedetomidine Hydrochloride", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA203972", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}