Budesonide 47335-0632-49

Package NDC

47335-0632-49

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Suspension
Route: Respiratory (inhalation)
Product Type: Human Prescription Drug
Marketing Start: May 1, 2021
Listing Expires: December 31, 2027
Application: ANDA211922

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Active Ingredients

Ingredient	Strength
Budesonide	.5 mg/2mL

Drug Class

Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]

Selected Package

47335-0632-49Selected

6 POUCH in 1 CARTON (47335-632-49) / 5 AMPULE in 1 POUCH (47335-632-48) / 2 mL in 1 AMPULE