Package 72572-127-10

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72572-127-10
Digits Only 7257212710
Product NDC 72572-127
Description

10 BOTTLE in 1 CARTON (72572-127-10) / 50 mL in 1 BOTTLE (72572-127-01)

Marketing

Marketing Status
Marketed Since 2021-08-23
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": "47eccaa8-c341-4a62-8de2-4fd36e010ed7", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["1faf1ac8-ff9b-4ed9-b562-06dab971173a"], "manufacturer_name": ["CIVICA, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BOTTLE in 1 CARTON (72572-127-10)  / 50 mL in 1 BOTTLE (72572-127-01)", "package_ndc": "72572-127-10", "marketing_start_date": "20210823"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "product_id": "72572-127_47eccaa8-c341-4a62-8de2-4fd36e010ed7", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "72572-127", "generic_name": "dexmedetomidine hydrochloride", "labeler_name": "CIVICA, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA212791", "marketing_category": "ANDA", "marketing_start_date": "20210823", "listing_expiration_date": "20261231"}