FDA Drug Approval, A208891, WIXELA INHUB
FDA Drug Approval, A208891, WIXELA INHUB
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$149.00 USD
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ANDA: 208891
Company: MYLAN
Drug Name: WIXELA INHUB
Active Ingredients: FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
Strength: 0.5MG/INH;EQ 0.05MG BASE/INH
Dosage Form/Route: POWDER;INHALATION
Action Date: 01/30/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: MYLAN
Drug Name: WIXELA INHUB
Active Ingredients: FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
Strength: 0.5MG/INH;EQ 0.05MG BASE/INH
Dosage Form/Route: POWDER;INHALATION
Action Date: 01/30/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB