Package 67457-924-50
Brand: dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloridePackage Facts
Identity
Package NDC
67457-924-50
Digits Only
6745792450
Product NDC
67457-924
Description
20 BOTTLE in 1 CARTON (67457-924-50) / 50 mL in 1 BOTTLE (67457-924-00)
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": "b51a1fb0-fcee-4a76-9eaf-91c35813c242", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["f140de5a-f13d-46b4-a742-049c63e474f5"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BOTTLE in 1 CARTON (67457-924-50) / 50 mL in 1 BOTTLE (67457-924-00)", "package_ndc": "67457-924-50", "marketing_start_date": "20201113"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "product_id": "67457-924_b51a1fb0-fcee-4a76-9eaf-91c35813c242", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "67457-924", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "200 ug/50mL"}], "application_number": "ANDA212571", "marketing_category": "ANDA", "marketing_start_date": "20201113", "listing_expiration_date": "20261231"}