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01 2ACETAZOLAMIDE

02 2AMINOCAPROIC ACID

03 3BACLOFEN

04 3BUMETANIDE

05 5CHLORPROMAZINE HYDROCHLORIDE

06 2CHLORTHALIDONE

07 2CHLORZOXAZONE

08 1CLINDAMYCIN PALMITATE HYDROCHLORIDE

09 1CLOMIPHENE CITRATE

10 1CYPROHEPTADINE HYDROCHLORIDE

11 4DOXAZOSIN MESYLATE

12 5DOXEPIN HYDROCHLORIDE

13 1FAMOTIDINE

14 2FLUOXETINE HYDROCHLORIDE

15 2GLYCOPYRROLATE

16 6HALOPERIDOL

17 4HYDROXYCHLOROQUINE SULFATE

18 3IRBESARTAN

19 4LABETALOL HYDROCHLORIDE

20 2LAMIVUDINE

21 2METRONIDAZOLE

22 2MODAFINIL

23 1NITROFURANTOIN

24 4PERPHENAZINE

25 3PRAZOSIN HYDROCHLORIDE

26 1RAMELTEON

27 2RANITIDINE HYDROCHLORIDE

28 3SERTRALINE HYDROCHLORIDE

29 3SILDENAFIL CITRATE

30 1VALGANCICLOVIR HYDROCHLORIDE

31 2VENLAFAXINE HYDROCHLORIDE

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PharmaCompass

01

Brand Name : ACETAZOLAMIDE

AACR Annual meeting
Not Confirmed
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Brand Name : ACETAZOLAMIDE

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AACR Annual meeting
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Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : ACETAZOLAMIDE

Dosage Strength : 125MG

Packaging :

Approval Date : 2021-02-22

Application Number : 211372

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : ACETAZOLAMIDE

AACR Annual meeting
Not Confirmed
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Brand Name : ACETAZOLAMIDE

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : ACETAZOLAMIDE

Dosage Strength : 250MG

Packaging :

Approval Date : 2021-02-22

Application Number : 211372

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : AMINOCAPROIC ACID

AACR Annual meeting
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : AMINOCAPROIC ACID

Dosage Strength : 500MG

Packaging :

Approval Date : 2022-09-14

Application Number : 213944

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : AMINOCAPROIC ACID

AACR Annual meeting
Not Confirmed
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Brand Name : AMINOCAPROIC ACID

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : AMINOCAPROIC ACID

Dosage Strength : 1GM

Packaging :

Approval Date : 2022-09-14

Application Number : 213944

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : BACLOFEN

AACR Annual meeting
Not Confirmed
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Brand Name : BACLOFEN

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BACLOFEN

Dosage Strength : 10MG

Packaging :

Approval Date : 2010-02-18

Application Number : 90334

Regulatory Info : DISCN

Registration Country : USA

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06

Brand Name : BACLOFEN

AACR Annual meeting
Not Confirmed
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Brand Name : BACLOFEN

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BACLOFEN

Dosage Strength : 20MG

Packaging :

Approval Date : 2010-02-18

Application Number : 90334

Regulatory Info : DISCN

Registration Country : USA

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07

Brand Name : BACLOFEN

AACR Annual meeting
Not Confirmed
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Brand Name : BACLOFEN

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BACLOFEN

Dosage Strength : 5MG

Packaging :

Approval Date : 2025-01-31

Application Number : 90334

Regulatory Info : RX

Registration Country : USA

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08

Brand Name : BUMETANIDE

AACR Annual meeting
Not Confirmed
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Brand Name : BUMETANIDE

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BUMETANIDE

Dosage Strength : 0.5MG

Packaging :

Approval Date : 2024-09-18

Application Number : 212931

Regulatory Info : RX

Registration Country : USA

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09

Brand Name : BUMETANIDE

AACR Annual meeting
Not Confirmed
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Brand Name : BUMETANIDE

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BUMETANIDE

Dosage Strength : 1MG

Packaging :

Approval Date : 2024-09-18

Application Number : 212931

Regulatory Info : RX

Registration Country : USA

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10

Brand Name : BUMETANIDE

AACR Annual meeting
Not Confirmed
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Brand Name : BUMETANIDE

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AACR Annual meeting
Not Confirmed

Appco Pharmaceutical Corp

Dosage Form : TABLET;ORAL

Brand Name : BUMETANIDE

Dosage Strength : 2MG

Packaging :

Approval Date : 2024-09-18

Application Number : 212931

Regulatory Info : RX

Registration Country : USA

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