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01 2ABIRATERONE ACETATE

02 1AMIKACIN SULFATE

03 1BORTEZOMIB

04 1BUMETANIDE

05 1CARFILZOMIB

06 4CEFAZOLIN SODIUM

07 3CEFEPIME HYDROCHLORIDE

08 5CEFTRIAXONE SODIUM

09 1CETRORELIX ACETATE

10 1CISPLATIN

11 1DAPTOMYCIN

12 1DECITABINE

13 1EXEMESTANE

14 1FOSAPREPITANT DIMEGLUMINE

15 1GEFITINIB

16 1HYDROXYUREA

17 2IMATINIB MESYLATE

18 3IRINOTECAN HYDROCHLORIDE

19 6LENALIDOMIDE

20 2MEROPENEM

21 6OLANZAPINE

22 3OLMESARTAN MEDOXOMIL

23 1ONDANSETRON HYDROCHLORIDE

24 5OXALIPLATIN

25 2PALONOSETRON HYDROCHLORIDE

26 2PEMETREXED DISODIUM

27 2SOLIFENACIN SUCCINATE

28 4TADALAFIL

29 3TENOFOVIR DISOPROXIL FUMARATE

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PharmaCompass

01

Brand Name : ABIRATERONE ACETATE

2024 ACI Convention
Not Confirmed
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Brand Name : ABIRATERONE ACETATE

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : TABLET; ORAL

Proprietary Name : ABIRATERONE ACETATE

Dosage Strength : 250MG

Approval Date : 2019-09-27

Application Number : 212462

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : ABIRATERONE ACETATE

2024 ACI Convention
Not Confirmed
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Brand Name : ABIRATERONE ACETATE

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : TABLET; ORAL

Proprietary Name : ABIRATERONE ACETATE

Dosage Strength : 500MG

Approval Date : 2021-06-25

Application Number : 212462

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : AMIKACIN SULFATE

2024 ACI Convention
Not Confirmed
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Brand Name : AMIKACIN SULFATE

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMIKACIN SULFATE

Dosage Strength : EQ 250MG BASE/ML

Approval Date : 2024-03-19

Application Number : 218146

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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04

Brand Name : BORTEZOMIB

2024 ACI Convention
Not Confirmed
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Brand Name : BORTEZOMIB

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INTRAVENOUS, SUBCU...

Proprietary Name : BORTEZOMIB

Dosage Strength : 3.5MG/VIAL

Approval Date : 2022-05-02

Application Number : 210824

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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05

Brand Name : BUMETANIDE

2024 ACI Convention
Not Confirmed
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Brand Name : BUMETANIDE

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : BUMETANIDE

Dosage Strength : 0.25MG/ML

Approval Date : 2024-09-19

Application Number : 219116

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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06

Brand Name : CARFILZOMIB

2024 ACI Convention
Not Confirmed
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Brand Name : CARFILZOMIB

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : POWDER; INTRAVENOUS

Proprietary Name : CARFILZOMIB

Dosage Strength : 60MG/VIAL

Approval Date :

Application Number : 209528

RX/OTC/DISCN :

RLD :

TE Code :

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07

Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFAZOLIN SODIUM

Dosage Strength : EQ 1GM BASE/VIAL

Approval Date : 2015-12-28

Application Number : 203661

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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08

Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFAZOLIN SODIUM

Dosage Strength : EQ 2GM BASE/VIAL

Approval Date : 2022-03-11

Application Number : 203661

RX/OTC/DISCN : RX

RLD : No

TE Code :

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09

Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
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Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFAZOLIN SODIUM

Dosage Strength : EQ 3GM BASE/VIAL

Approval Date : 2024-01-24

Application Number : 203661

RX/OTC/DISCN : RX

RLD : No

TE Code :

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10

Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
arrow

Brand Name : CEFAZOLIN SODIUM

2024 ACI Convention
Not Confirmed
arrow

Qilu Pharmaceutical

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFAZOLIN SODIUM

Dosage Strength : EQ 10GM BASE/VIAL

Approval Date : 2018-10-17

Application Number : 209217

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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