Labetalol Hydrochloride 72572-0350
Product NDC
72572-0350- Manufacturer
- Civica, Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- November 21, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA075303
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 5 mg/mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
1 VIAL in 1 BOX, UNIT-DOSE (72572-350-01) / 20 mL in 1 VIAL