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01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE

02 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE

03 1CIPROFLOXACIN HYDROCHLORIDE

04 1DEXAMETHASONE

05 4FENOPROFEN CALCIUM

06 1VORAPAXAR SULFATE

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PharmaCompass

01

Brand Name : BUTALBITAL, ACETAMIN...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : BUTALBITAL, ACETAMIN...

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : CAPSULE; ORAL

Proprietary Name : BUTALBITAL, ACETAMINOPHE...

Dosage Strength : 300MG;50MG;40MG

Approval Date : 2017-08-04

Application Number : 206615

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Brand Name : TREZIX

Pharmtech & Ingredients
Not Confirmed
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Brand Name : TREZIX

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : CAPSULE; ORAL

Proprietary Name : TREZIX

Dosage Strength : 320.5MG;30MG;16MG

Approval Date : 2014-11-26

Application Number : 204785

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Brand Name : CETRAXAL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : CETRAXAL

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : SOLUTION/DROPS; OTIC

Proprietary Name : CETRAXAL

Dosage Strength : EQ 0.2% BASE

Approval Date : 2009-05-01

Application Number : 21918

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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04

Brand Name : DEXAMETHASONE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DEXAMETHASONE

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : TABLET; ORAL

Proprietary Name : DEXAMETHASONE

Dosage Strength : 1.5MG

Approval Date : 1983-04-28

Application Number : 88237

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
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Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : CAPSULE; ORAL

Proprietary Name : NALFON

Dosage Strength : EQ 300MG BASE **Federal ...

Approval Date : 1982-01-01

Application Number : 17604

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
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Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
arrow

Key Therapeutics

Dosage Form : CAPSULE; ORAL

Proprietary Name : NALFON

Dosage Strength : EQ 200MG BASE

Approval Date : 1982-01-01

Application Number : 17604

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
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Brand Name : NALFON

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : CAPSULE; ORAL

Proprietary Name : NALFON

Dosage Strength : EQ 400MG BASE

Approval Date : 2009-07-21

Application Number : 17604

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Brand Name : FENOPROFEN CALCIUM

Pharmtech & Ingredients
Not Confirmed
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Brand Name : FENOPROFEN CALCIUM

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : TABLET; ORAL

Proprietary Name : FENOPROFEN CALCIUM

Dosage Strength : EQ 600MG BASE

Approval Date : 1988-08-17

Application Number : 72267

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Brand Name : ZONTIVITY

Pharmtech & Ingredients
Not Confirmed
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Brand Name : ZONTIVITY

Pharmtech & Ingredients
Not Confirmed
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Key Therapeutics

Dosage Form : TABLET; ORAL

Proprietary Name : ZONTIVITY

Dosage Strength : EQ 2.08MG BASE

Approval Date : 2014-05-08

Application Number : 204886

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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