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01 4ALBUTEROL SULFATE

02 2ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

03 2BUDESONIDE

04 1IPRATROPIUM BROMIDE

05 1ISOETHARINE HYDROCHLORIDE

06 1KETOROLAC TROMETHAMINE

07 2METAPROTERENOL SULFATE

08 2SODIUM CHLORIDE

09 1STERILE WATER FOR INJECTION

10 2VERAPAMIL HYDROCHLORIDE

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PharmaCompass

01

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
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Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.083% BASE

Approval Date : 1997-09-17

Application Number : 74880

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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02

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
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Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.5% BASE

Approval Date : 2001-06-26

Application Number : 75664

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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03

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.042% BASE

Approval Date : 2004-06-28

Application Number : 76355

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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04

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : ALBUTEROL SULFATE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.021% BASE

Approval Date : 2010-03-31

Application Number : 76355

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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05

Brand Name : ALBUTEROL SULFATE AN...

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ALBUTEROL SULFATE AN...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE AND IP...

Dosage Strength : EQ 0.083% BASE;0.017%

Approval Date : 2007-12-31

Application Number : 76749

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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06

Brand Name : ALBUTEROL SULFATE; I...

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ALBUTEROL SULFATE; I...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : ALBUTEROL SULFATE; IPRAT...

Dosage Strength : 0.5MG; 0.017%

Approval Date :

Application Number : 76749

RX/OTC/DISCN :

RLD :

TE Code :

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07

Brand Name : BUDESONIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BUDESONIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Nephron Pharmaceuticals Corporation

Dosage Form : SUSPENSION; INHALATION

Proprietary Name : BUDESONIDE

Dosage Strength : 0.25MG/2ML

Approval Date : 2009-03-30

Application Number : 78202

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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08

Brand Name : BUDESONIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BUDESONIDE

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Nephron Pharmaceuticals Corporation

Dosage Form : SUSPENSION; INHALATION

Proprietary Name : BUDESONIDE

Dosage Strength : 0.5MG/2ML

Approval Date : 2009-03-30

Application Number : 78202

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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09

Brand Name : IPRATROPIUM BROMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : IPRATROPIUM BROMIDE

Pharma, Lab & Chemical Expo
Not Confirmed
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Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : IPRATROPIUM BROMIDE

Dosage Strength : 0.02%

Approval Date : 2001-09-27

Application Number : 75562

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

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10

Brand Name : BETA-2

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : BETA-2

Pharma, Lab & Chemical Expo
Not Confirmed
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Nephron Pharmaceuticals Corporation

Dosage Form : SOLUTION; INHALATION

Proprietary Name : BETA-2

Dosage Strength : 1%

Approval Date : 1982-01-01

Application Number : 86711

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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