Labetalol Hydrochloride 83301-0059
Product NDC
83301-0059- Manufacturer
- Mullan Pharmaceutical Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA090699
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 200 mg/40mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
1 VIAL, MULTI-DOSE in 1 CARTON (83301-0059-1) / 40 mL in 1 VIAL, MULTI-DOSE