Package 0338-9555-24

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0338-9555-24
Digits Only 0338955524
Product NDC 0338-9555
Description

24 BAG in 1 CARTON (0338-9555-24) / 50 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2018-08-21
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": "594e9faa-bc32-42e0-9c0a-8fa9460b1e24", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["8ccb45a7-8290-469c-9644-a4dca967d88f"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-9555-24)  / 50 mL in 1 BAG", "package_ndc": "0338-9555-24", "marketing_start_date": "20180821"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "product_id": "0338-9555_594e9faa-bc32-42e0-9c0a-8fa9460b1e24", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "0338-9555", "generic_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "200 ug/50mL"}], "application_number": "ANDA208532", "marketing_category": "ANDA", "marketing_start_date": "20180821", "listing_expiration_date": "20271231"}