Esmolol Hydrochloride 51662-1322
Product NDC
51662-1322- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 19, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA076474
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Esmolol Hydrochloride | 10 mg/mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
10 mL in 1 VIAL (51662-1322-1)