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01 5AstraZeneca
02 1B. Braun Medical
03 2DENTSPLY PHARM
04 1Dentsply Detrey Gmbh
05 1Polifarma
06 2SEPTODONT INC
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01 9INJECTABLE;INJECTION
02 2Injectable Solution
03 1Solution for IV Injection
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01 1Approved
02 1Authorized
03 6DISCN
04 3RX
05 1Blank
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01 3CITANEST
02 1CITANEST FORTE
03 1CITANEST FORTE DENTAL
04 1CITANEST PLAIN
05 1CITANEST PLAIN DENTAL
06 1Citanest Dental Octapressin
07 1PRILOCAINE HYDROCHLORIDE
08 1PRILOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE
09 1Takipril Hiperbarica
10 1Blank
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01 1Spain
02 1Sweden
03 1Turkey
04 9USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITANEST
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITANEST PLAIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
EPINEPHRINE BITARTRATE; PRILOCAINE HYDROCHLORIDE
Brand Name : CITANEST FORTE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;4%
Packaging :
Approval Date : 1982-01-01
Application Number : 14763
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Takipril Hiperbarica
Dosage Form : Injectable Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 2012-10-18
Application Number : 70932
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CITANEST PLAIN DENTAL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4%
Packaging :
Approval Date : 1982-01-01
Application Number : 21382
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
EPINEPHRINE BITARTRATE; PRILOCAINE HYDROCHLORIDE
Brand Name : CITANEST FORTE DENTAL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;4%
Packaging :
Approval Date : 1982-01-01
Application Number : 21383
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Turkey
Brand Name :
Dosage Form : Solution for IV Injection
Dosage Strength : 2%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info : RX
Registration Country : USA
EPINEPHRINE BITARTRATE; PRILOCAINE HYDROCHLORIDE
Brand Name : PRILOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.005MG/ML;4%
Packaging :
Approval Date : 2011-08-30
Application Number : 78959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRILOCAINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4%
Packaging :
Approval Date : 2010-09-29
Application Number : 79235
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
Felypressin; Prilocaine Hydrochloride
Brand Name : Citanest Dental Octapressin
Dosage Form : Injectable Solution
Dosage Strength : 30mg/ml;0.54mcg/ml
Packaging :
Approval Date : 29/08/1986
Application Number : 19860829000098
Regulatory Info : Approved
Registration Country : Sweden
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