"0093-7868-65" National Drug Code (NDC)

Fentanyl Citrate 30 BLISTER PACK in 1 CARTON (0093-7868-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7868-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7868-65
Package Description30 BLISTER PACK in 1 CARTON (0093-7868-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7868-19)
Product NDC0093-7868
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFentanyl Citrate
Non-Proprietary NameFentanyl Citrate
Dosage FormLOZENGE
UsageORAL; TRANSMUCOSAL
Start Marketing Date20151208
End Marketing Date20260831
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020747
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFENTANYL CITRATE
Strength800
Strength Unitug/1
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII

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