Package 0409-3382-21

Brand: sufentanil citrate

Generic: sufentanil citrate
NDC Package

Package Facts

Identity

Package NDC 0409-3382-21
Digits Only 0409338221
Product NDC 0409-3382
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (0409-3382-21) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-3382-11)

Marketing

Marketing Status
Marketed Since 2005-07-26
Brand sufentanil citrate
Generic sufentanil citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INTRAVENOUS"], "spl_id": "589d789c-2fbd-40ee-bbe4-8906afa2062d", "openfda": {"unii": ["S9ZFX8403R"], "rxcui": ["1809097", "1809102", "1809104"], "spl_set_id": ["20293943-46ff-4345-1aa4-929b4e017a25"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-3382-21)  / 1 mL in 1 VIAL, SINGLE-DOSE (0409-3382-11)", "package_ndc": "0409-3382-21", "marketing_start_date": "20050726"}], "brand_name": "Sufentanil Citrate", "product_id": "0409-3382_589d789c-2fbd-40ee-bbe4-8906afa2062d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0409-3382", "dea_schedule": "CII", "generic_name": "SUFENTANIL CITRATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sufentanil Citrate", "active_ingredients": [{"name": "SUFENTANIL CITRATE", "strength": "50 ug/mL"}], "application_number": "ANDA074534", "marketing_category": "ANDA", "marketing_start_date": "20050726", "listing_expiration_date": "20261231"}