Package 71872-7031-1

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7031-1
Digits Only 7187270311
Product NDC 71872-7031
Description

1 VIAL in 1 BAG (71872-7031-1) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-03-02
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": "fd1604d4-5081-7e98-e053-6394a90af8aa", "openfda": {"upc": ["0371872703116"], "unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["a268e759-9a3e-1d7b-e053-2a95a90a335b"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7031-1)  / 2 mL in 1 VIAL", "package_ndc": "71872-7031-1", "marketing_start_date": "20200302"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "71872-7031_fd1604d4-5081-7e98-e053-6394a90af8aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71872-7031", "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": "ANDA205867", "marketing_category": "ANDA", "marketing_start_date": "20160317", "listing_expiration_date": "20261231"}