Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 3MANKIND PHARMA
02 3CIPLA
03 4HIKMA
04 3IMPAX LABS INC
05 4LUOXIN AUROVITAS
06 1MYLAN SPECIALITY LP
07 2NEPHRON
08 3PHARMOBEDIENT
09 3RITEDOSE CORP
10 3SUN PHARM
11 1TEVA PARENTERAL
12 3TEVA PHARMS USA
01 33SOLUTION;INHALATION
01 13DISCN
02 18RX
03 2Blank
01 29LEVALBUTEROL HYDROCHLORIDE
02 4XOPENEX
01 27No
02 4Yes
03 2Blank
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code :
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.0103% BASE
Approval Date : 2024-10-21
Application Number : 218770
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code :
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.021% BASE
Approval Date : 2024-10-21
Application Number : 218770
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code :
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.042% BASE
Approval Date : 2024-10-21
Application Number : 218770
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 0.021% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1999-03-25
Application Number : 20837
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 0.042% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1999-03-25
Application Number : 20837
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 0.0103% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-01-30
Application Number : 20837
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 2003-07-18
Application Number : 20837
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AN
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.021% BASE
Approval Date : 2008-04-09
Application Number : 77756
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
RLD : No
TE Code : AN
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.042% BASE
Approval Date : 2008-04-09
Application Number : 77756
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
RLD : No
TE Code : AN
Brand Name : LEVALBUTEROL HYDROCHLORIDE
Dosage Form : SOLUTION;INHALATION
Dosage Strength : EQ 0.0103% BASE
Approval Date : 2008-04-09
Application Number : 77756
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
