Package 70069-759-04

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-759-04
Digits Only 7006975904
Product NDC 70069-759
Product ID 70069-759_6a1a2c33-1467-4eb0-adc6-6e21771fbf6b
Description

4 VIAL in 1 CARTON (70069-759-04) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-09-26
Brand dexmedetomidine hydrochloride
Generic dexmedetomidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmedetomidine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "6a1a2c33-1467-4eb0-adc6-6e21771fbf6b", "openfda": {"upc": ["0370069759011", "0370069759042", "0370069758045", "0370069758014"], "unii": ["1018WH7F9I"], "rxcui": ["1788947"], "spl_set_id": ["649e777b-9b30-4f1e-9fb9-6bba57580976"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (70069-759-04)  / 10 mL in 1 VIAL", "package_ndc": "70069-759-04", "marketing_start_date": "20240926"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "70069-759_6a1a2c33-1467-4eb0-adc6-6e21771fbf6b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "70069-759", "generic_name": "Dexmedetomidine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA218112", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}