Dobutamine 70436-0203
Product NDC
70436-0203- Manufacturer
- Slate Run Pharmaceuticals
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA216131
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dobutamine Hydrochloride | 250 mg/20mL |
Drug Class
Adrenergic beta-Agonists [MoA]beta-Adrenergic Agonist [EPC]
Packaging Options(2)
1 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-80) / 20 mL in 1 VIAL, SINGLE-DOSE
10 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-82) / 20 mL in 1 VIAL, SINGLE-DOSE