loader
Please Wait
Applying Filters...

Approved Drug Products of Chirhoclin listed in the FDA Orange Book. Original Data : FDA Website

Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2PORCINE SECRETIN

02 2SECRETIN SYNTHETIC HUMAN

03 1SECRETIN SYNTHETIC PORCINE

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass
Left Arrow
Right Arrow

01

Brand Name : PORCINE SECRETIN

Discovery on Target
Not Confirmed
arrow

Brand Name : PORCINE SECRETIN

Discovery on Target
Not Confirmed
arrow

CHIRHOCLIN

Dosage Form : INJECTABLE; SUBCUTANEOUS LYOPH...

Proprietary Name : PORCINE SECRETIN

Dosage Strength : 16MCG

Approval Date :

Application Number : 21209

RX/OTC/DISCN :

RLD :

TE Code :

blank

02

Brand Name : PORCINE SECRETIN

Luxepack
Not Confirmed
arrow

Brand Name : PORCINE SECRETIN

Luxepack
Not Confirmed
arrow

CHIRHOCLIN

Dosage Form : INJECTABLE; SUBCUTANEOUS LYOPH...

Proprietary Name : PORCINE SECRETIN

Dosage Strength : 40MCG

Approval Date :

Application Number : 21209

RX/OTC/DISCN :

RLD :

TE Code :

blank

03

Brand Name : CHIRHOSTIM

Luxepack
Not Confirmed
arrow

Brand Name : CHIRHOSTIM

Luxepack
Not Confirmed
arrow

CHIRHOCLIN

Dosage Form : FOR SOLUTION; INTRAVENOUS

Proprietary Name : CHIRHOSTIM

Dosage Strength : 16MCG/VIAL

Approval Date : 2004-04-09

Application Number : 21256

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

04

Brand Name : CHIRHOSTIM

Luxepack
Not Confirmed
arrow

Brand Name : CHIRHOSTIM

Luxepack
Not Confirmed
arrow

CHIRHOCLIN

Dosage Form : FOR SOLUTION; INTRAVENOUS

Proprietary Name : CHIRHOSTIM

Dosage Strength : 40MCG/VIAL

Approval Date : 2007-06-21

Application Number : 21256

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

05

Brand Name : SECREFLO

Luxepack
Not Confirmed
arrow

Brand Name : SECREFLO

Luxepack
Not Confirmed
arrow

CHIRHOCLIN

Dosage Form : FOR SOLUTION; INTRAVENOUS

Proprietary Name : SECREFLO

Dosage Strength : 16MCG/VIAL

Approval Date : 2002-04-04

Application Number : 21136

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank