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01 1ACYCLOVIR SODIUM

02 1AZITHROMYCIN

03 1BIVALIRUDIN

04 2CILOSTAZOL

05 3CINACALCET HYDROCHLORIDE

06 1DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE

07 1DICYCLOMINE HYDROCHLORIDE

08 1DOBUTAMINE HYDROCHLORIDE

09 2DOXYCYCLINE HYCLATE

10 2EPLERENONE

11 2EPTIFIBATIDE

12 1ESOMEPRAZOLE SODIUM

13 2FLUOXETINE HYDROCHLORIDE

14 1GANCICLOVIR SODIUM

15 1LINCOMYCIN HYDROCHLORIDE

16 5LURASIDONE HYDROCHLORIDE

17 1METHOCARBAMOL

18 4SODIUM NITROPRUSSIDE

19 2TETRABENAZINE

20 1TOBRAMYCIN SULFATE

21 4VANCOMYCIN HYDROCHLORIDE

22 1VORICONAZOLE

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PharmaCompass

01

Brand Name : ACYCLOVIR SODIUM

2024 ACI Convention
Not Confirmed
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Brand Name : ACYCLOVIR SODIUM

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE;INJECTION

Brand Name : ACYCLOVIR SODIUM

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 2024-01-08

Application Number : 218111

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : AZITHROMYCIN

2024 ACI Convention
Not Confirmed
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Brand Name : AZITHROMYCIN

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE;INJECTION

Brand Name : AZITHROMYCIN

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2018-10-09

Application Number : 203412

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : BIVALIRUDIN

2024 ACI Convention
Not Confirmed
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Brand Name : BIVALIRUDIN

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE;INTRAVENOUS

Brand Name : BIVALIRUDIN

Dosage Strength : 250MG/VIAL

Packaging :

Approval Date : 2021-05-28

Application Number : 213078

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : CILOSTAZOL

2024 ACI Convention
Not Confirmed
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Brand Name : CILOSTAZOL

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CILOSTAZOL

Dosage Strength : 100MG

Packaging :

Approval Date : 2006-03-29

Application Number : 77208

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : CILOSTAZOL

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Not Confirmed
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Brand Name : CILOSTAZOL

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CILOSTAZOL

Dosage Strength : 50MG

Packaging :

Approval Date : 2006-03-29

Application Number : 77208

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : CINACALCET HYDROCHLO...

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Not Confirmed
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Brand Name : CINACALCET HYDROCHLO...

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CINACALCET HYDROCHLORIDE

Dosage Strength : EQ 30MG BASE

Packaging :

Approval Date : 2018-08-01

Application Number : 210207

Regulatory Info : RX

Registration Country : USA

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07

Brand Name : CINACALCET HYDROCHLO...

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Not Confirmed
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Brand Name : CINACALCET HYDROCHLO...

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CINACALCET HYDROCHLORIDE

Dosage Strength : EQ 60MG BASE

Packaging :

Approval Date : 2018-08-01

Application Number : 210207

Regulatory Info : RX

Registration Country : USA

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08

Brand Name : CINACALCET HYDROCHLO...

2024 ACI Convention
Not Confirmed
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Brand Name : CINACALCET HYDROCHLO...

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CINACALCET HYDROCHLORIDE

Dosage Strength : EQ 90MG BASE

Packaging :

Approval Date : 2018-08-01

Application Number : 210207

Regulatory Info : RX

Registration Country : USA

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09

Brand Name : PROMETHAZINE DM

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Not Confirmed
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Brand Name : PROMETHAZINE DM

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : SYRUP;ORAL

Brand Name : PROMETHAZINE DM

Dosage Strength : 15MG/5ML;6.25MG/5ML

Packaging :

Approval Date : 2006-02-14

Application Number : 40649

Regulatory Info : RX

Registration Country : USA

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10

Brand Name : DICYCLOMINE HYDROCHL...

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Not Confirmed
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Brand Name : DICYCLOMINE HYDROCHL...

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2024 ACI Convention
Not Confirmed

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE;INJECTION

Brand Name : DICYCLOMINE HYDROCHLORIDE

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 2018-11-02

Application Number : 207076

Regulatory Info : RX

Registration Country : USA

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