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01 1ARSENIC TRIOXIDE

02 1BUSULFAN

03 1COLISTIMETHATE SODIUM

04 2CYCLOPHOSPHAMIDE

05 1DICYCLOMINE HYDROCHLORIDE

06 2EPHEDRINE SULFATE

07 1ERYTHROMYCIN LACTOBIONATE

08 2FLUORESCEIN SODIUM

09 1ISOPROTERENOL HYDROCHLORIDE

10 3LEVETIRACETAM

11 1MINOCYCLINE

12 1NELARABINE

13 6POTASSIUM CHLORIDE

14 2PROCAINAMIDE HYDROCHLORIDE

15 1PROCHLORPERAZINE EDISYLATE

16 2SODIUM CHLORIDE

17 1SODIUM NITROPRUSSIDE

18 2STERILE WATER FOR INJECTION

19 1SUCCINYLCHOLINE CHLORIDE

20 1TESTOSTERONE ENANTHATE

21 2TIROFIBAN HYDROCHLORIDE

22 1TRANEXAMIC ACID

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PharmaCompass

01

Brand Name : ARSENIC TRIOXIDE

2024 ACI Convention
Not Confirmed
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Brand Name : ARSENIC TRIOXIDE

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ARSENIC TRIOXIDE

Dosage Strength : 1MG/ML

Approval Date : 2018-11-15

Application Number : 209780

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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02

Brand Name : BUSULFAN

2024 ACI Convention
Not Confirmed
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Brand Name : BUSULFAN

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : BUSULFAN

Dosage Strength : 6MG/ML

Approval Date : 2019-01-14

Application Number : 207794

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Brand Name : COLISTIMETHATE SODIU...

2024 ACI Convention
Not Confirmed
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Brand Name : COLISTIMETHATE SODIU...

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : COLISTIMETHATE SODIUM

Dosage Strength : EQ 150MG BASE/VIAL

Approval Date : 2004-03-19

Application Number : 65177

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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04

Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CYCLOPHOSPHAMIDE

Dosage Strength : 500MG/2.5ML(200MG/ML)

Approval Date :

Application Number : 216783

RX/OTC/DISCN :

RLD :

TE Code :

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05

Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CYCLOPHOSPHAMIDE

Dosage Strength : 1G/5ML(200MG/ML)

Approval Date :

Application Number : 216783

RX/OTC/DISCN :

RLD :

TE Code :

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06

Brand Name : DICYCLOMINE HYDROCHL...

2024 ACI Convention
Not Confirmed
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Brand Name : DICYCLOMINE HYDROCHL...

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DICYCLOMINE HYDROCHLORID...

Dosage Strength : 10MG/ML

Approval Date : 2019-02-01

Application Number : 206468

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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07

Brand Name : EMERPHED

2024 ACI Convention
Not Confirmed
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Brand Name : EMERPHED

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : EMERPHED

Dosage Strength : 50MG/10ML (5MG/ML)

Approval Date : 2020-04-17

Application Number : 213407

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

Brand Name : EMERPHED

2024 ACI Convention
Not Confirmed
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Brand Name : EMERPHED

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : EMERPHED

Dosage Strength : 25MG/5ML (5MG/ML)

Approval Date : 2023-02-28

Application Number : 213407

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

Brand Name : ERYTHROMYCIN LACTOBI...

2024 ACI Convention
Not Confirmed
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Brand Name : ERYTHROMYCIN LACTOBI...

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ERYTHROMYCIN LACTOBIONAT...

Dosage Strength : EQ 500MG BASE/VIAL

Approval Date : 2022-02-14

Application Number : 215290

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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10

Brand Name : FLUORESCEIN SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : FLUORESCEIN SODIUM

2024 ACI Convention
Not Confirmed
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Nexus Pharmaceuticals

Dosage Form : INJECTABLE; INTRAVENOUS

Proprietary Name : FLUORESCEIN SODIUM

Dosage Strength : EQ 500MG BASE/5ML (EQ 10...

Approval Date : 2023-09-25

Application Number : 215709

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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