fentanyl

Generic: fentanyl

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fentanyl
Generic Name fentanyl
Labeler ingenus pharmaceuticals, llc
Dosage Form PATCH, EXTENDED RELEASE
Routes
TRANSDERMAL
Active Ingredients

fentanyl 50 ug/h

Manufacturer
INGENUS PHARMACEUTICALS, LLC

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)
opioid agonist [epc]
Mechanism of Action
full opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742552
Hyphenated Format 50742-552

Supplemental Identifiers

RxCUI
197696 245134 245135 245136 577057 1603495 1603498 1603501
UNII
UF599785JZ
NUI
N0000175684 N0000175690

Packaging Origin

Original Packager
true

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
TRANSDERMAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/h
source: ndc
Packaging
  • 5 POUCH in 1 CARTON (50742-552-05) / 1 PATCH in 1 POUCH (50742-552-01) / 72 h in 1 PATCH
source: ndc

Packages (1)

Ingredients (1)

fentanyl (50 ug/h)

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"}