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01 3Mankind Pharma

02 3Cipla

03 4Hikma Pharmaceuticals

04 3Impax Laboratories

05 4Luoxin Pharmaceutical

06 3PHARMOBEDIENT

07 3Sun Pharmaceutical Industries Limited

08 4Teva Pharmaceutical Industries

09 3The Ritedose Corporation

10 1Viatris

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : DISCN

Registration Country : USA

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE

Packaging :

Approval Date : 2024-10-21

Application Number : 218770

Regulatory Info : DISCN

Registration Country : USA

Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : DISCN

Registration Country : USA

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE

Packaging :

Approval Date : 2024-10-21

Application Number : 218770

Regulatory Info : DISCN

Registration Country : USA

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : DISCN

Registration Country : USA

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE

Packaging :

Approval Date : 2024-10-21

Application Number : 218770

Regulatory Info : DISCN

Registration Country : USA

Company Banner

04

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE

Packaging :

Approval Date : 2013-12-13

Application Number : 78171

Regulatory Info : RX

Registration Country : USA

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05

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE

Packaging :

Approval Date : 2013-12-13

Application Number : 78171

Regulatory Info : RX

Registration Country : USA

blank

06

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE

Packaging :

Approval Date : 2013-12-13

Application Number : 78171

Regulatory Info : RX

Registration Country : USA

blank

07

Organic Process R&D
Not Confirmed
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arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : XOPENEX

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-03-25

Application Number : 20837

Regulatory Info : DISCN

Registration Country : USA

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08

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : XOPENEX

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-03-25

Application Number : 20837

Regulatory Info : DISCN

Registration Country : USA

blank

09

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : XOPENEX

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2002-01-30

Application Number : 20837

Regulatory Info : DISCN

Registration Country : USA

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10

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : XOPENEX

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.25% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2003-07-18

Application Number : 20837

Regulatory Info : DISCN

Registration Country : USA

blank

11

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE

Packaging :

Approval Date : 2008-04-09

Application Number : 77756

Regulatory Info : RX

Registration Country : USA

blank

12

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE

Packaging :

Approval Date : 2008-04-09

Application Number : 77756

Regulatory Info : RX

Registration Country : USA

blank

13

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE

Packaging :

Approval Date : 2008-04-09

Application Number : 77756

Regulatory Info : RX

Registration Country : USA

blank

14

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE

Packaging :

Approval Date : 2013-04-26

Application Number : 90297

Regulatory Info : RX

Registration Country : USA

blank

15

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE

Packaging :

Approval Date : 2013-04-26

Application Number : 90297

Regulatory Info : RX

Registration Country : USA

blank

16

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE

Packaging :

Approval Date : 2013-04-26

Application Number : 90297

Regulatory Info : RX

Registration Country : USA

blank

17

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.25% BASE

Packaging :

Approval Date : 2009-03-20

Application Number : 78309

Regulatory Info : RX

Registration Country : USA

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18

PHARMOBEDIENT

Country
PackExpo
Not Confirmed
arrow

PHARMOBEDIENT

Country
arrow
PackExpo
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.0103% BASE

Packaging :

Approval Date : 2013-03-15

Application Number : 77800

Regulatory Info : DISCN

Registration Country : USA

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19

PHARMOBEDIENT

Country
PackExpo
Not Confirmed
arrow

PHARMOBEDIENT

Country
arrow
PackExpo
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.021% BASE

Packaging :

Approval Date : 2013-03-15

Application Number : 77800

Regulatory Info : DISCN

Registration Country : USA

blank

20

PHARMOBEDIENT

Country
PackExpo
Not Confirmed
arrow

PHARMOBEDIENT

Country
arrow
PackExpo
Not Confirmed

LEVALBUTEROL HYDROCHLORIDE

Brand Name : LEVALBUTEROL HYDROCHLORIDE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : EQ 0.042% BASE

Packaging :

Approval Date : 2013-03-15

Application Number : 77800

Regulatory Info : DISCN

Registration Country : USA

blank