NDC 0406-9175

FENTANYL TRANSDERMAL

Fentanyl Transdermal

FENTANYL TRANSDERMAL is a Transdermal Patch, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Specgx Llc. The primary component is Fentanyl.

Product ID0406-9175_301a8c6d-a664-4eac-9c9e-8c47eb34dae4
NDC0406-9175
Product TypeHuman Prescription Drug
Proprietary NameFENTANYL TRANSDERMAL
Generic NameFentanyl Transdermal
Dosage FormPatch, Extended Release
Route of AdministrationTRANSDERMAL
Marketing Start Date2020-05-06
Marketing CategoryANDA / ANDA
Application NumberANDA077154
Labeler NameSpecGx LLC
Substance NameFENTANYL
Active Ingredient Strength75 ug/h
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0406-9175-76

5 POUCH in 1 CARTON (0406-9175-76) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Marketing Start Date2020-05-06
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "FENTANYL TRANSDERMAL" or generic name "Fentanyl Transdermal"

NDCBrand NameGeneric Name
0406-9000FENTANYL TRANSDERMALfentanyl transdermal
0406-9012FENTANYL TRANSDERMALfentanyl transdermal
0406-9025FENTANYL TRANSDERMALfentanyl transdermal
0406-9037FENTANYL TRANSDERMALfentanyl transdermal
0406-9050FENTANYL TRANSDERMALfentanyl transdermal
0406-9062FENTANYL TRANSDERMALfentanyl transdermal
0406-9075FENTANYL TRANSDERMALfentanyl transdermal
0406-9100FENTANYL TRANSDERMALfentanyl transdermal
0406-9112FENTANYL TRANSDERMALfentanyl transdermal
0406-9125FENTANYL TRANSDERMALfentanyl transdermal
0406-9150FENTANYL TRANSDERMALfentanyl transdermal
0406-9175FENTANYL TRANSDERMALfentanyl transdermal
63629-4764FENTANYL TRANSDERMALfentanyl transdermal
63629-4771FENTANYL TRANSDERMALfentanyl transdermal
63629-4773FENTANYL TRANSDERMALfentanyl transdermal

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