Package 83634-600-02

Brand: dexmedetomidine

Generic: dexmedetomidine
NDC Package

Package Facts

Identity

Package NDC 83634-600-02
Digits Only 8363460002
Product NDC 83634-600
Description

25 VIAL in 1 CARTON (83634-600-02) / 2 mL in 1 VIAL (83634-600-41)

Marketing

Marketing Status
Marketed Since 2024-03-15
Brand dexmedetomidine
Generic dexmedetomidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3e30e931-4d42-465c-9e4b-cd3137ba5fe2", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["eee6145b-d83f-4596-92d3-733934d8a3a4"], "manufacturer_name": ["Avenacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (83634-600-02)  / 2 mL in 1 VIAL (83634-600-41)", "package_ndc": "83634-600-02", "marketing_start_date": "20240315"}], "brand_name": "Dexmedetomidine", "product_id": "83634-600_3e30e931-4d42-465c-9e4b-cd3137ba5fe2", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "83634-600", "generic_name": "dexmedetomidine", "labeler_name": "Avenacy Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA209065", "marketing_category": "ANDA", "marketing_start_date": "20240315", "listing_expiration_date": "20261231"}