Package 0143-9391-10

Brand: remifentanil hydrochloride

Generic: remifentanil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9391-10
Digits Only 0143939110
Product NDC 0143-9391
Product ID 0143-9391_5c5e498b-d829-4f78-bcca-466631014767
Description

10 VIAL in 1 CARTON (0143-9391-10) / 3 mL in 1 VIAL (0143-9391-01)

Marketing

Marketing Status
Marketed Since 2021-05-15
Brand remifentanil hydrochloride
Generic remifentanil hydrochloride
Sample Package No

Linked Drug Pages (1)

REMIFENTANIL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5c5e498b-d829-4f78-bcca-466631014767", "openfda": {"unii": ["5V444H5WIC"], "rxcui": ["1729578", "1729584", "1729710"], "spl_set_id": ["9d289052-1eb6-4ba2-a3ca-d2e542a052ae"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9391-10)  / 3 mL in 1 VIAL (0143-9391-01)", "package_ndc": "0143-9391-10", "marketing_start_date": "20210515"}], "brand_name": "REMIFENTANIL HYDROCHLORIDE", "product_id": "0143-9391_5c5e498b-d829-4f78-bcca-466631014767", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0143-9391", "dea_schedule": "CII", "generic_name": "REMIFENTANIL HYDROCHLORIDE", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "REMIFENTANIL HYDROCHLORIDE", "active_ingredients": [{"name": "REMIFENTANIL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA210594", "marketing_category": "ANDA", "marketing_start_date": "20210515", "listing_expiration_date": "20261231"}