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01 1ACETAZOLAMIDE SODIUM

02 1AMPHOTERICIN B

03 1BACITRACIN

04 1BACITRACIN ZINC

05 2CLONIDINE HYDROCHLORIDE

06 3CYCLOPHOSPHAMIDE

07 1DACTINOMYCIN

08 1FOLIC ACID

09 1HYDROCORTISONE

10 1HYDROCORTISONE ACETATE

11 1IBUPROFEN LYSINE

12 1LEVETIRACETAM

13 1LINCOMYCIN HYDROCHLORIDE

14 1LIOTHYRONINE SODIUM

15 1NELARABINE

16 2NEOMYCIN SULFATE

17 2NEOMYCIN SULFATE; POLYMYXIN B SULFATE

18 2PENTAMIDINE ISETHIONATE

19 1POLYMYXIN B SULFATE

20 2PROMETHAZINE HYDROCHLORIDE

21 1STREPTOMYCIN SULFATE

22 1TOBRAMYCIN SULFATE

23 1TRANEXAMIC ACID

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PharmaCompass

01

Brand Name : ACETAZOLAMIDE SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : ACETAZOLAMIDE SODIUM

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ACETAZOLAMIDE SODIUM

Dosage Strength : EQ 500MG BASE/VIAL

Approval Date : 2008-12-10

Application Number : 40784

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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02

Brand Name : AMPHOTERICIN B

2024 ACI Convention
Not Confirmed
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Brand Name : AMPHOTERICIN B

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMPHOTERICIN B

Dosage Strength : 50MG/VIAL

Approval Date : 1992-04-29

Application Number : 63206

RX/OTC/DISCN : RX

RLD : No

TE Code :

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03

Brand Name : BACI-RX

2024 ACI Convention
Not Confirmed
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Brand Name : BACI-RX

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : POWDER; FOR RX COMPOUNDING

Proprietary Name : BACI-RX

Dosage Strength : 5,000,000 UNITS/BOT

Approval Date : 1982-01-01

Application Number : 61580

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Brand Name : ZIBA-RX

2024 ACI Convention
Not Confirmed
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Brand Name : ZIBA-RX

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : POWDER; FOR RX COMPOUNDING

Proprietary Name : ZIBA-RX

Dosage Strength : 500,000 UNITS/BOT

Approval Date : 1982-01-01

Application Number : 61737

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : CLONIDINE HYDROCHLOR...

2024 ACI Convention
Not Confirmed
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Brand Name : CLONIDINE HYDROCHLOR...

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CLONIDINE HYDROCHLORIDE

Dosage Strength : 1MG/10ML (0.1MG/ML)

Approval Date : 2013-10-29

Application Number : 203167

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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06

Brand Name : CLONIDINE HYDROCHLOR...

2024 ACI Convention
Not Confirmed
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Brand Name : CLONIDINE HYDROCHLOR...

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CLONIDINE HYDROCHLORIDE

Dosage Strength : 5MG/10ML (0.5MG/ML)

Approval Date : 2013-10-29

Application Number : 203167

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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07

Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CYCLOPHOSPHAMIDE

Dosage Strength : 500MG/VIAL

Approval Date : 2022-10-18

Application Number : 211757

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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08

Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CYCLOPHOSPHAMIDE

Dosage Strength : 1GM/VIAL

Approval Date : 2022-10-18

Application Number : 211757

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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09

Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CYCLOPHOSPHAMIDE

Dosage Strength : 2GM/VIAL

Approval Date : 2022-10-18

Application Number : 211757

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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10

Brand Name : DACTINOMYCIN

2024 ACI Convention
Not Confirmed
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Brand Name : DACTINOMYCIN

2024 ACI Convention
Not Confirmed
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XGen Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DACTINOMYCIN

Dosage Strength : 0.5MG/VIAL

Approval Date : 2019-05-20

Application Number : 203999

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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