Home NDC 60505-7006-0 NDC 60505-7006-0 - FENTANYL This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 60505-7006
Requested NDC 60505-7006-0
Package NDCs from labels 60505-7006-0, 60505-7006-2
Manufacturer Bryant Ranch Prepack
Effective date 2023-07-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60505-7006 FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 17 Legacy NDC 20230714_0ff70df0-2cda-d96c-42a8-3bf180310498.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded FENTANYL ACTIVE INGREDIENT UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 FENTANYL ACTIVE MOIETY UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 OCTYLDODECANOL INACTIVE INGREDIENT 461N1O614Y FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 POLYBUTENE (1400 MW) INACTIVE INGREDIENT 1NA5AO9GH7 FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 POLYISOBUTYLENE (800000 MW) INACTIVE INGREDIENT Y132ZOQ9H7 FENTANYL PATCH, EXTENDED RELEASE [BRYANT RANCH PREPACK] 1000 FENTANYL ACTIVE INGREDIENT UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 FENTANYL ACTIVE MOIETY UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 OCTYLDODECANOL INACTIVE INGREDIENT 461N1O614Y FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 POLYBUTENE (1400 MW) INACTIVE INGREDIENT 1NA5AO9GH7 FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 POLYISOBUTYLENE (800000 MW) INACTIVE INGREDIENT Y132ZOQ9H7 FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] 5 FENTANYL ACTIVE INGREDIENT UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1 FENTANYL ACTIVE MOIETY UF599785JZ FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1 OCTYLDODECANOL INACTIVE INGREDIENT 461N1O614Y FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1 POLYBUTENE (1400 MW) INACTIVE INGREDIENT 1NA5AO9GH7 FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1 POLYISOBUTYLENE (800000 MW) INACTIVE INGREDIENT Y132ZOQ9H7 FENTANYL PATCH, EXTENDED RELEASE [DIRECTRX] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 ยท 10 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join FENTANYL TRANSDERMAL FENTANYL TRANSDERMAL SpecGx LLC e15a7e9b-8025-49dd-9a6d-bafcccf1959f 2026-04-30 Boxed warning, Warnings, Adverse reactions Exact identifier rxcui: 245134 unii: UF599785JZ FENTANYL FENTANYL Aveva Drug Delivery Systems Inc. 73897c38-e4ec-40bc-9f41-3359ee23a5a8 2026-04-07 Boxed warning, Warnings, Adverse reactions Exact identifier application number: ANDA077449 rxcui: 245134 unii: UF599785JZ FENTANYL FENTANYL INGENUS PHARMACEUTICALS, LLC bf02ffd0-cc5d-446b-b648-378f6885052f 2026-04-07 Boxed warning, Warnings, Adverse reactions Exact identifier application number: ANDA077449 rxcui: 245134 unii: UF599785JZ Fentanyl system FENTANYL ALVOGEN 242759ef-cb6d-4e3e-9f8d-5e31efa1f289 2026-03-02 Boxed warning, Warnings, Adverse reactions Exact identifier rxcui: 245134 unii: UF599785JZ FENTANYL FENTANYL Mylan Pharmaceuticals Inc. 2a2238e9-4b5d-c56d-8663-dd354ff9ae0c 2025-12-15 Boxed warning, Warnings, Adverse reactions Exact identifier rxcui: 245134 unii: UF599785JZ 005d170d-692f-f040-e063-6394a90aa0a4 0ff70df0-2cda-d96c-42a8-3bf180310498 2023-07-13 Boxed warning, Warnings, Adverse reactions Exact identifier spl id: 005d170d-692f-f040-e063-6394a90aa0a4 spl set id: 0ff70df0-2cda-d96c-42a8-3bf180310498 005ffedc-9d49-b5cb-e063-6394a90af21c 7c51f184-c2a0-4867-b8fb-d58910ee1966 2023-07-13 Boxed warning, Warnings, Adverse reactions Exact identifier spl id: 005ffedc-9d49-b5cb-e063-6394a90af21c spl set id: 7c51f184-c2a0-4867-b8fb-d58910ee1966 7cc2dbb3-4aec-4e03-bf14-89c9de8fd2cb 911c67e4-7eb0-4f42-9d14-749995a3e6f5 2023-03-20 Boxed warning, Warnings, Adverse reactions Exact identifier spl set id: 911c67e4-7eb0-4f42-9d14-749995a3e6f5 9c9402dc-ee5b-6c1f-e053-2995a90adabd bcf3d225-2404-4cf5-8a58-bb8f27fe2a35 2020-01-20 Boxed warning, Warnings, Adverse reactions Exact identifier spl id: 9c9402dc-ee5b-6c1f-e053-2995a90adabd spl set id: bcf3d225-2404-4cf5-8a58-bb8f27fe2a35 cdb0d55e-4716-4fc3-b837-7c68cacbb91d ad0b6309-dbfc-4e54-b6a1-0fe95a7ad6a0 2017-02-16 Boxed warning, Warnings, Adverse reactions Exact identifier spl id: cdb0d55e-4716-4fc3-b837-7c68cacbb91d spl set id: ad0b6309-dbfc-4e54-b6a1-0fe95a7ad6a0
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.