Package 25021-617-82

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-617-82
Digits Only 2502161782
Product NDC 25021-617
Description

20 BAG in 1 CARTON (25021-617-82) / 100 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2025-07-15
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": "56ca6ba0-864c-4360-8791-0bd8399b2a2b", "openfda": {"upc": ["0325021617823"], "unii": ["1018WH7F9I"], "rxcui": ["1718909"], "spl_set_id": ["65885aef-faaf-4dec-a180-9a657f738bbc"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CARTON (25021-617-82)  / 100 mL in 1 BAG", "package_ndc": "25021-617-82", "marketing_start_date": "20250715"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "25021-617_56ca6ba0-864c-4360-8791-0bd8399b2a2b", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "25021-617", "generic_name": "Dexmedetomidine Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA209307", "marketing_category": "ANDA", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}