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01 4NOVARTIS
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01 4TABLET;ORAL
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01 4RX
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01 4ZORTRESS
01 4Yes
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RLD : Yes
TE Code : AB
Novartis Pharmaceuticals Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : ZORTRESS
Dosage Strength : 0.25MG
Approval Date : 2010-04-20
Application Number : 21560
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
RLD : Yes
TE Code : AB
Novartis Pharmaceuticals Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : ZORTRESS
Dosage Strength : 1MG
Approval Date : 2018-08-10
Application Number : 21560
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
RLD : Yes
TE Code : AB
Novartis Pharmaceuticals Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : ZORTRESS
Dosage Strength : 0.5MG
Approval Date : 2010-04-20
Application Number : 21560
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
RLD : Yes
TE Code : AB
Novartis Pharmaceuticals Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : ZORTRESS
Dosage Strength : 0.75MG
Approval Date : 2010-04-20
Application Number : 21560
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
