Labetalol Hydrochloride 68001-0701-03
- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 15, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA074787
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 200 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Selected Package
68001-0701-03Selected500 TABLET in 1 BOTTLE (68001-701-03)
Other packages for this product(1)
100 TABLET in 1 BOTTLE (68001-701-00)