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01 1ACETAZOLAMIDE SODIUM

02 1AMPHOTERICIN B

03 1BACITRACIN

04 1BACITRACIN ZINC

05 2CLONIDINE HYDROCHLORIDE

06 3CYCLOPHOSPHAMIDE

07 1DACTINOMYCIN

08 2EDARAVONE

09 1FOLIC ACID

10 1HYDROCORTISONE

11 1HYDROCORTISONE ACETATE

12 1IBUPROFEN LYSINE

13 1LEVETIRACETAM

14 1LINCOMYCIN HYDROCHLORIDE

15 1LIOTHYRONINE SODIUM

16 1NELARABINE

17 2NEOMYCIN SULFATE

18 2NEOMYCIN SULFATE; POLYMYXIN B SULFATE

19 2PENTAMIDINE ISETHIONATE

20 1POLYMYXIN B SULFATE

21 2PROMETHAZINE HYDROCHLORIDE

22 1STREPTOMYCIN SULFATE

23 1TOBRAMYCIN SULFATE

24 1TRANEXAMIC ACID

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PharmaCompass

01

Brand Name : ACETAZOLAMIDE SODIUM

Antibody Engineering
Not Confirmed
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Brand Name : ACETAZOLAMIDE SODIUM

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : AMPHOTERICIN B

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : BACI-RX

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : ZIBA-RX

Antibody Engineering
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...

Antibody Engineering
Not Confirmed
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Brand Name : CLONIDINE HYDROCHLOR...

Antibody Engineering
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...

Antibody Engineering
Not Confirmed
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Brand Name : CLONIDINE HYDROCHLOR...

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : CYCLOPHOSPHAMIDE

Antibody Engineering
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

Antibody Engineering
Not Confirmed
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Brand Name : DACTINOMYCIN

Antibody Engineering
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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