Budesonide 47335-0633
Product NDC
47335-0633- 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 | 1 mg/2mL |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
6 POUCH in 1 CARTON (47335-633-49) / 5 AMPULE in 1 POUCH (47335-633-48) / 2 mL in 1 AMPULE