Package 71872-7122-1
Brand: dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloridePackage Facts
Identity
Package NDC
71872-7122-1
Digits Only
7187271221
Product NDC
71872-7122
Description
1 VIAL, SINGLE-DOSE in 1 BAG (71872-7122-1) / 2 mL in 1 VIAL, SINGLE-DOSE
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": "fc5dd4b0-0e31-858e-e053-6394a90a2714", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["6937235f-ea25-4950-e053-2991aa0a9b74"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7122-1) / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7122-1", "marketing_start_date": "20180330"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "71872-7122_fc5dd4b0-0e31-858e-e053-6394a90a2714", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71872-7122", "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": "ANDA202126", "marketing_category": "ANDA", "marketing_start_date": "20150408", "listing_expiration_date": "20261231"}