Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.
01 3MISSION PHARMA
02 3STRIDES PHARMA
03 2ANI PHARMS
04 3ASCENT PHARMS INC
05 2BIONPHARMA
06 3HIBROW HLTHCARE
07 2RISING
08 3TEVA PHARMS USA INC
09 3TORRENT
10 2UT SW MEDCTR
11 3ZYDUS PHARMS
01 2FOR SOLUTION;ORAL
02 27TABLET, EXTENDED RELEASE;ORAL
01 5DISCN
02 24RX
01 26POTASSIUM CITRATE
02 3UROCIT-K
01 24No
02 5Yes
Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.
RLD : Yes
TE Code : AB
Brand Name : UROCIT-K
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MEQ
Approval Date : 1985-08-30
Application Number : 19071
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
Brand Name : POTASSIUM CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MEQ
Approval Date : 2017-09-11
Application Number : 206813
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.
RLD : Yes
TE Code : AB
Brand Name : UROCIT-K
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MEQ
Approval Date : 1992-08-31
Application Number : 19071
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.
RLD : Yes
TE Code : AB
Brand Name : UROCIT-K
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 15MEQ
Approval Date : 2009-12-30
Application Number : 19071
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
Brand Name : POTASSIUM CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MEQ
Approval Date : 2017-09-11
Application Number : 206813
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
Brand Name : POTASSIUM CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 15MEQ
Approval Date : 2017-09-11
Application Number : 206813
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : POTASSIUM CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MEQ
Approval Date : 2006-06-09
Application Number : 77440
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : POTASSIUM CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MEQ
Approval Date : 2006-06-09
Application Number : 77440
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : POTASSIUM CITRATE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-10-13
Application Number : 19647
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : POTASSIUM CITRATE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 10MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-10-13
Application Number : 19647
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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