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01 4ALPRAZOLAM

02 3AMLODIPINE BESYLATE

03 1ASPIRIN; CARISOPRODOL

04 1ASPIRIN; CARISOPRODOL; CODEINE PHOSPHATE

05 2BACLOFEN

06 3BENZTROPINE MESYLATE

07 4BUSPIRONE HYDROCHLORIDE

08 4CAPTOPRIL

09 1CARISOPRODOL

10 2CYCLOBENZAPRINE HYDROCHLORIDE

11 3DIPYRIDAMOLE

12 2ETODOLAC

13 2GLIPIZIDE

14 2GLYCOPYRROLATE

15 2HYDROCHLOROTHIAZIDE

16 3IMIPRAMINE HYDROCHLORIDE

17 3LEVETIRACETAM

18 3LORAZEPAM

19 2METHOCARBAMOL

20 3METHYLPHENIDATE HYDROCHLORIDE

21 2NABUMETONE

22 4PAROXETINE HYDROCHLORIDE

23 2PRIMIDONE

24 1RIFAMPIN

25 3SERTRALINE HYDROCHLORIDE

26 5SIMVASTATIN

27 4SOTALOL HYDROCHLORIDE

28 3SPIRONOLACTONE

29 2TIZANIDINE HYDROCHLORIDE

30 2TRAZODONE HYDROCHLORIDE

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PharmaCompass

01

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
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Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
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Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : ALPRAZOLAM

Dosage Strength : 0.25MG

Approval Date : 2008-09-25

Application Number : 78491

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : ALPRAZOLAM

Dosage Strength : 0.5MG

Approval Date : 2008-09-25

Application Number : 78491

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : ALPRAZOLAM

Dosage Strength : 1MG

Approval Date : 2008-09-25

Application Number : 78491

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Brand Name : ALPRAZOLAM

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : ALPRAZOLAM

Dosage Strength : 2MG

Approval Date : 2008-12-12

Application Number : 78491

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : AMLODIPINE BESYLATE

Dosage Strength : EQ 2.5MG BASE

Approval Date : 2010-04-07

Application Number : 78414

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : AMLODIPINE BESYLATE

Dosage Strength : EQ 5MG BASE

Approval Date : 2010-04-07

Application Number : 78414

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : AMLODIPINE BESYLATE

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : AMLODIPINE BESYLATE

Dosage Strength : EQ 10MG BASE

Approval Date : 2010-04-07

Application Number : 78414

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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08

Brand Name : CARISOPRODOL AND ASP...

BioFlorida Conference
Not Confirmed
arrow

Brand Name : CARISOPRODOL AND ASP...

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : CARISOPRODOL AND ASPIRIN

Dosage Strength : 325MG;200MG

Approval Date : 1997-12-10

Application Number : 40252

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Brand Name : CARISOPRODOL, ASPIRI...

BioFlorida Conference
Not Confirmed
arrow

Brand Name : CARISOPRODOL, ASPIRI...

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : CARISOPRODOL, ASPIRIN AN...

Dosage Strength : 325MG;200MG;16MG

Approval Date : 1998-12-29

Application Number : 40283

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Brand Name : BACLOFEN

BioFlorida Conference
Not Confirmed
arrow

Brand Name : BACLOFEN

BioFlorida Conference
Not Confirmed
arrow

Oxford Pharm

Dosage Form : TABLET; ORAL

Proprietary Name : BACLOFEN

Dosage Strength : 20MG

Approval Date : 2007-10-31

Application Number : 77088

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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