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01 2ACETAZOLAMIDE

02 2AMINOCAPROIC ACID

03 2BACLOFEN

04 3BUMETANIDE

05 5CHLORPROMAZINE HYDROCHLORIDE

06 2CHLORTHALIDONE

07 1CLINDAMYCIN PALMITATE HYDROCHLORIDE

08 1CLOMIPHENE CITRATE

09 1CYPROHEPTADINE HYDROCHLORIDE

10 5DOXEPIN HYDROCHLORIDE

11 2GLYCOPYRROLATE

12 4HYDROXYCHLOROQUINE SULFATE

13 4LABETALOL HYDROCHLORIDE

14 2METRONIDAZOLE

15 2MODAFINIL

16 4PERPHENAZINE

17 3PRAZOSIN HYDROCHLORIDE

18 2RANITIDINE HYDROCHLORIDE

19 3SERTRALINE HYDROCHLORIDE

20 3SILDENAFIL CITRATE

21 1VALGANCICLOVIR HYDROCHLORIDE

22 2VENLAFAXINE HYDROCHLORIDE

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PharmaCompass

01

Brand Name : ACETAZOLAMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ACETAZOLAMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : ACETAZOLAMIDE

Dosage Strength : 125MG

Approval Date : 2021-02-22

Application Number : 211372

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : ACETAZOLAMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ACETAZOLAMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : ACETAZOLAMIDE

Dosage Strength : 250MG

Approval Date : 2021-02-22

Application Number : 211372

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : AMINOCAPROIC ACID

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

Pharma, Lab & Chemical Expo
Not Confirmed
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Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 500MG

Approval Date : 2022-09-14

Application Number : 213944

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : AMINOCAPROIC ACID

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : AMINOCAPROIC ACID

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 1GM

Approval Date : 2022-09-14

Application Number : 213944

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

Brand Name : BACLOFEN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BACLOFEN

Pharma, Lab & Chemical Expo
Not Confirmed
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Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : BACLOFEN

Dosage Strength : 10MG

Approval Date : 2010-02-18

Application Number : 90334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Brand Name : BACLOFEN

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BACLOFEN

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : BACLOFEN

Dosage Strength : 20MG

Approval Date : 2010-02-18

Application Number : 90334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : BUMETANIDE

Dosage Strength : 0.5MG

Approval Date : 2024-09-18

Application Number : 212931

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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08

Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : BUMETANIDE

Dosage Strength : 1MG

Approval Date : 2024-09-18

Application Number : 212931

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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09

Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : BUMETANIDE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : BUMETANIDE

Dosage Strength : 2MG

Approval Date : 2024-09-18

Application Number : 212931

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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10

Brand Name : CHLORPROMAZINE HYDRO...

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : CHLORPROMAZINE HYDRO...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Appco Pharmaceutical Corp

Dosage Form : TABLET; ORAL

Proprietary Name : CHLORPROMAZINE HYDROCHLO...

Dosage Strength : 10MG

Approval Date : 2020-08-31

Application Number : 213590

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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