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"70839-359-04" National Drug Code (NDC)
Goprelto 1 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASS
(LXO US Inc.)
NDC Code
70839-359-04
Package Description
1 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASS
Product NDC
70839-359
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Goprelto
Non-Proprietary Name
Cocaine Hydrochloride
Dosage Form
SOLUTION
Usage
NASAL
Start Marketing Date
20240209
Marketing Category Name
NDA
Application Number
NDA209963
Manufacturer
LXO US Inc.
Substance Name
COCAINE HYDROCHLORIDE
Strength
40
Strength Unit
mg/mL
DEA Schedule
CII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70839-359-04