Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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01 1STRIDES PHARMA
02 1AIZANT
03 1ANNORA PHARMA
04 3CHIESI
05 1LUPIN LTD
06 1RISING
07 1TEVA PHARMS USA
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01 7TABLET, EXTENDED RELEASE;ORAL
02 2TABLET;ORAL
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01 4DISCN
02 5RX
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01 6ZILEUTON
02 2ZYFLO
03 1ZYFLO CR
01 7No
02 2Yes
RLD : No
TE Code : AB
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2019-12-16
Application Number : 212670
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2020-10-23
Application Number : 211390
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2022-10-11
Application Number : 215742
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : ZYFLO
Dosage Form : TABLET;ORAL
Dosage Strength : 300MG
Approval Date : 1996-12-09
Application Number : 20471
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : ZYFLO
Dosage Form : TABLET;ORAL
Dosage Strength : 600MG
Approval Date : 1996-12-09
Application Number : 20471
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ZYFLO CR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-05-30
Application Number : 22052
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2019-11-05
Application Number : 211972
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2017-03-17
Application Number : 204929
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : ZILEUTON
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2022-05-03
Application Number : 211043
RX/OTC/DISCN : DISCN
RLD : No
TE Code :