fentanyl
Generic: fentanyl
Labeler: ingenus pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
fentanyl
Generic Name
fentanyl
Labeler
ingenus pharmaceuticals, llc
Dosage Form
PATCH, EXTENDED RELEASE
Routes
Active Ingredients
fentanyl 50 ug/h
Manufacturer
Identifiers & Regulatory
Product NDC
50742-552
Product ID
50742-552_43e1addf-2ed8-d034-e063-6294a90aa1bd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077449
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2025-01-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50742552
Hyphenated Format
50742-552
Supplemental Identifiers
RxCUI
UNII
NUI
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
fentanyl (source: ndc)
Generic Name
fentanyl (source: ndc)
Application Number
ANDA077449 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/h
Packaging
- 5 POUCH in 1 CARTON (50742-552-05) / 1 PATCH in 1 POUCH (50742-552-01) / 72 h in 1 PATCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TRANSDERMAL"], "spl_id": "43e1addf-2ed8-d034-e063-6294a90aa1bd", "openfda": {"nui": ["N0000175684", "N0000175690"], "unii": ["UF599785JZ"], "rxcui": ["197696", "245134", "245135", "245136", "577057", "1603495", "1603498", "1603501"], "spl_set_id": ["bf02ffd0-cc5d-446b-b648-378f6885052f"], "pharm_class_epc": ["Opioid Agonist [EPC]"], "pharm_class_moa": ["Full Opioid Agonists [MoA]"], "manufacturer_name": ["INGENUS PHARMACEUTICALS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (50742-552-05) / 1 PATCH in 1 POUCH (50742-552-01) / 72 h in 1 PATCH", "package_ndc": "50742-552-05", "marketing_start_date": "20250106"}], "brand_name": "FENTANYL", "product_id": "50742-552_43e1addf-2ed8-d034-e063-6294a90aa1bd", "dosage_form": "PATCH, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50742-552", "dea_schedule": "CII", "generic_name": "FENTANYL", "labeler_name": "INGENUS PHARMACEUTICALS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENTANYL", "active_ingredients": [{"name": "FENTANYL", "strength": "50 ug/h"}], "application_number": "ANDA077449", "marketing_category": "ANDA", "marketing_start_date": "20250106", "listing_expiration_date": "20261231"}