Budesonide 68682-0309
Product NDC
68682-0309- Manufacturer
- Oceanside Pharmaceuticals
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 10, 2018
- Listing Expires
- December 31, 2026
- Application
- NDA203634
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Budesonide | 9 mg/1 |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)