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 3NORVIUM BIOSCIENCE
08 3RITEDOSE CORP
09 3SUN PHARM
10 1TEVA PARENTERAL
11 3TEVA PHARMS USA
01 31SOLUTION;INHALATION
01 10DISCN
02 21RX
01 27LEVALBUTEROL HYDROCHLORIDE
02 4XOPENEX
01 27No
02 4Yes
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AN
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 : RX
RLD : No
TE Code : AN
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AN
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 : RX
RLD : No
TE Code : AN
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AN
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 : RX
RLD : No
TE Code : AN
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Dosage Strength : EQ 0.021% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 0.042% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 0.0103% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
