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AstraZeneca’s Pulmicort Respules Inhalation Suspension

Lupin gets FDA approval for budesonide inhalation suspension

Lupin gets FDA approval for budesonide inhalation suspension

MUMBAI, India and BALTIMORE, Md. — Pharma major Lupin announced that it has received approval for its budesonide inhalation suspension, 0.5 mg/2 mL single-dose ampules from the United States Food and Drug Administration to market a generic version of AstraZeneca Pharmaceuticals LP’s (AstraZeneca) Pulmicort Respules Inhalation Suspension, 0.5 mg/2 mL. Lupin’s budesonide inhalation suspension, 0.5

PP_1170x120_10-25-21