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Approved Drug Products of Assia Chemical Industries Ltd listed in the FDA Orange Book. Original Data : FDA Website

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01 3CABOZANTINIB

02 1CETRORELIX ACETATE

03 4ELTROMBOPAG CHOLINE

04 1HYDROCORTISONE

05 1MESALAMINE

06 1PACLITAXEL

07 1PAZOPANIB HYDROCHLORIDE

08 1TADALAFIL

09 2THEOPHYLLINE

10 2TIOPRONIN

11 2VALBENAZINE TOSYLATE

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01

Brand Name : CABOZANTINIB

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02

Brand Name : CABOZANTINIB

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03

Brand Name : CABOZANTINIB

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04

Brand Name : CETRORELIX ACETATE

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Brand Name : CETRORELIX ACETATE

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Assia Chemical Industries Ltd

Dosage Form : POWDER; SUBCUTANEOUS

Proprietary Name : CETRORELIX ACETATE

Dosage Strength : EQ 0.25MG BASE/VIAL

Approval Date : 2022-08-12

Application Number : 215737

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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05

Brand Name : ALVAIZ

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Brand Name : ALVAIZ

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Assia Chemical Industries Ltd

Dosage Form : TABLET; ORAL

Proprietary Name : ALVAIZ

Dosage Strength : EQ 9MG BASE

Approval Date : 2023-11-29

Application Number : 216774

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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06

Brand Name : ALVAIZ

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Brand Name : ALVAIZ

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Assia Chemical Industries Ltd

Dosage Form : TABLET; ORAL

Proprietary Name : ALVAIZ

Dosage Strength : EQ 18MG BASE

Approval Date : 2023-11-29

Application Number : 216774

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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07

Brand Name : ALVAIZ

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Brand Name : ALVAIZ

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Assia Chemical Industries Ltd

Dosage Form : TABLET; ORAL

Proprietary Name : ALVAIZ

Dosage Strength : EQ 36MG BASE

Approval Date : 2023-11-29

Application Number : 216774

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

Brand Name : ALVAIZ

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Brand Name : ALVAIZ

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Assia Chemical Industries Ltd

Dosage Form : TABLET; ORAL

Proprietary Name : ALVAIZ

Dosage Strength : EQ 54MG BASE

Approval Date : 2023-11-29

Application Number : 216774

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

Brand Name : ACTICORT

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Brand Name : ACTICORT

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Assia Chemical Industries Ltd

Dosage Form : LOTION; TOPICAL

Proprietary Name : ACTICORT

Dosage Strength : 1%

Approval Date : 1982-01-01

Application Number : 86535

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Brand Name : MESALAMINE

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Brand Name : MESALAMINE

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Assia Chemical Industries Ltd

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Proprietary Name : MESALAMINE

Dosage Strength : 800MG

Approval Date : 2024-08-22

Application Number : 213191

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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