Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1ACYCLOVIR SODIUM

02 1AZITHROMYCIN

03 1BIVALIRUDIN

04 2CILOSTAZOL

05 1DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE

06 1DICYCLOMINE HYDROCHLORIDE

07 1DOBUTAMINE HYDROCHLORIDE

08 2DOXYCYCLINE HYCLATE

09 2EPTIFIBATIDE

10 1ESOMEPRAZOLE SODIUM

11 1GANCICLOVIR SODIUM

12 1LINCOMYCIN HYDROCHLORIDE

13 1METHOCARBAMOL

14 4SODIUM NITROPRUSSIDE

15 1TOBRAMYCIN SULFATE

16 4VANCOMYCIN HYDROCHLORIDE

17 1VORICONAZOLE

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Brand Name : ACYCLOVIR SODIUM

ELCC
Not Confirmed
arrow

Brand Name : ACYCLOVIR SODIUM

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ACYCLOVIR SODIUM

Dosage Strength : EQ 50MG BASE/ML

Approval Date : 2024-01-08

Application Number : 218111

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

02

Brand Name : AZITHROMYCIN

ELCC
Not Confirmed
arrow

Brand Name : AZITHROMYCIN

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AZITHROMYCIN

Dosage Strength : EQ 500MG BASE/VIAL

Approval Date : 2018-10-09

Application Number : 203412

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

03

Brand Name : BIVALIRUDIN

ELCC
Not Confirmed
arrow

Brand Name : BIVALIRUDIN

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INTRAVENOUS

Proprietary Name : BIVALIRUDIN

Dosage Strength : 250MG/VIAL

Approval Date : 2021-05-28

Application Number : 213078

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

04

Brand Name : CILOSTAZOL

ELCC
Not Confirmed
arrow

Brand Name : CILOSTAZOL

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : CILOSTAZOL

Dosage Strength : 100MG

Approval Date : 2006-03-29

Application Number : 77208

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

05

Brand Name : CILOSTAZOL

ELCC
Not Confirmed
arrow

Brand Name : CILOSTAZOL

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : TABLET; ORAL

Proprietary Name : CILOSTAZOL

Dosage Strength : 50MG

Approval Date : 2006-03-29

Application Number : 77208

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

06

Brand Name : PROMETHAZINE DM

ELCC
Not Confirmed
arrow

Brand Name : PROMETHAZINE DM

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : SYRUP; ORAL

Proprietary Name : PROMETHAZINE DM

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

Approval Date : 2006-02-14

Application Number : 40649

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

blank

07

Brand Name : DICYCLOMINE HYDROCHL...

ELCC
Not Confirmed
arrow

Brand Name : DICYCLOMINE HYDROCHL...

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DICYCLOMINE HYDROCHLORID...

Dosage Strength : 10MG/ML

Approval Date : 2018-11-02

Application Number : 207076

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

08

Brand Name : DOBUTAMINE HYDROCHLO...

ELCC
Not Confirmed
arrow

Brand Name : DOBUTAMINE HYDROCHLO...

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DOBUTAMINE HYDROCHLORIDE

Dosage Strength : EQ 12.5MG BASE/ML

Approval Date : 2022-12-21

Application Number : 216131

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

09

Brand Name : DOXYCYCLINE HYCLATE

ELCC
Not Confirmed
arrow

Brand Name : DOXYCYCLINE HYCLATE

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DOXYCYCLINE HYCLATE

Dosage Strength : EQ 100MG BASE/VIAL

Approval Date : 2024-06-21

Application Number : 217685

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

10

Brand Name : DOXYCYCLINE HYCLATE

ELCC
Not Confirmed
arrow

Brand Name : DOXYCYCLINE HYCLATE

ELCC
Not Confirmed
arrow

Slate Run Pharmaceuticals

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : DOXYCYCLINE HYCLATE

Dosage Strength : EQ 200MG BASE/VIAL

Approval Date : 2024-06-21

Application Number : 217685

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank