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"0093-7870-65" National Drug Code (NDC)

Fentanyl Citrate 30 BLISTER PACK in 1 CARTON (0093-7870-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7870-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7870-65
Package Description30 BLISTER PACK in 1 CARTON (0093-7870-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7870-19)
Product NDC0093-7870
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFentanyl Citrate
Non-Proprietary NameFentanyl Citrate
Dosage FormLOZENGE
UsageORAL; TRANSMUCOSAL
Start Marketing Date20151208
End Marketing Date20260531
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020747
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFENTANYL CITRATE
Strength1600
Strength Unitug/1
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7870-65





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