01 5ASTRAZENECA
02 1DENTSPLY PHARM
01 6INJECTABLE;INJECTION
01 6DISCN
01 6DURANEST
01 6Yes
RLD : Yes
TE Code :
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17751
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
EPINEPHRINE; ETIDOCAINE HYDROCHLORIDE
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17751
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17751
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17751
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17751
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
EPINEPHRINE BITARTRATE; ETIDOCAINE HYDROCHLORIDE
Brand Name : DURANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 21384
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
