Package 71872-7030-1
Brand: dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloridePackage Facts
Identity
Package NDC
71872-7030-1
Digits Only
7187270301
Product NDC
71872-7030
Description
1 VIAL in 1 BAG (71872-7030-1) / 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": "fd163116-8854-9366-e053-6394a90a00b5", "openfda": {"upc": ["0371872703017"], "unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["a2666c50-3b55-1380-e053-2a95a90aea58"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7030-1) / 2 mL in 1 VIAL", "package_ndc": "71872-7030-1", "marketing_start_date": "20200228"}], "brand_name": "Dexmedetomidine hydrochloride", "product_id": "71872-7030_fd163116-8854-9366-e053-6394a90a00b5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71872-7030", "generic_name": "Dexmedetomidine hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA204023", "marketing_category": "ANDA", "marketing_start_date": "20161221", "listing_expiration_date": "20261231"}