"61919-602-05" National Drug Code (NDC)

Fentanyl 72 h in 1 PATCH (61919-602-05)
(DirectRX)

NDC Code61919-602-05
Package Description72 h in 1 PATCH (61919-602-05)
Product NDC61919-602
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFentanyl
Non-Proprietary NameFentanyl
Dosage FormPATCH, EXTENDED RELEASE
UsageTRANSDERMAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA077449
ManufacturerDirectRX
Substance NameFENTANYL
Strength25
Strength Unitug/h
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII

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