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Approved Drug Products containing 206309 listed in the FDA Orange Book. Original Data : FDA Website

FDA Orange Book

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01 6RISING PHARMA

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PharmaCompass

01

Brand Name : TEMOZOLOMIDE

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Not Confirmed
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Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 180MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 100MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 5MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
arrow

Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 250MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
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Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
arrow

Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 140MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
arrow

Brand Name : TEMOZOLOMIDE

Luxepack
Not Confirmed
arrow

Dosage Form : CAPSULE; ORAL

Proprietary Name : TEMOZOLOMIDE

Dosage Strength : 20MG

Approval Date : 2016-04-27

Application Number : 206309

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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