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"0093-7869-65" National Drug Code (NDC)
Fentanyl Citrate 30 BLISTER PACK in 1 CARTON (0093-7869-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7869-19)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-7869-65
Package Description
30 BLISTER PACK in 1 CARTON (0093-7869-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7869-19)
Product NDC
0093-7869
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fentanyl Citrate
Non-Proprietary Name
Fentanyl Citrate
Dosage Form
LOZENGE
Usage
ORAL; TRANSMUCOSAL
Start Marketing Date
20151208
End Marketing Date
20251031
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA020747
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
FENTANYL CITRATE
Strength
1200
Strength Unit
ug/1
Pharmacy Classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule
CII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7869-65