sufentanil citrate
Generic: sufentanil citrate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
sufentanil citrate
Generic Name
sufentanil citrate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sufentanil citrate 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-3382
Product ID
0409-3382_589d789c-2fbd-40ee-bbe4-8906afa2062d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074534
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2005-07-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04093382
Hyphenated Format
0409-3382
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sufentanil citrate (source: ndc)
Generic Name
sufentanil citrate (source: ndc)
Application Number
ANDA074534 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-3382-21) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-3382-11)
Packages (1)
Ingredients (1)
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"}