Package 84549-493-95

Brand: dexmedetomidine hydrochloride in 0.9% sodium chloride

Generic: dexmedetomidine hydrochloride in 0.9% sodium chloride
NDC Package

Package Facts

Identity

Package NDC 84549-493-95
Digits Only 8454949395
Product NDC 84549-493
Product ID 84549-493_42caba25-dd88-040c-e063-6294a90a7a12
Description

20 mL in 1 VIAL (84549-493-95)

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand dexmedetomidine hydrochloride in 0.9% sodium chloride
Generic dexmedetomidine hydrochloride in 0.9% sodium chloride
Sample Package No

Linked Drug Pages (1)

DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "42caba25-dd88-040c-e063-6294a90a7a12", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718900"], "spl_set_id": ["42caba25-dd87-040c-e063-6294a90a7a12"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL (84549-493-95)", "package_ndc": "84549-493-95", "marketing_start_date": "20251010"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE", "product_id": "84549-493_42caba25-dd88-040c-e063-6294a90a7a12", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "84549-493", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA209065", "marketing_category": "ANDA", "marketing_start_date": "20200612", "listing_expiration_date": "20261231"}