Labetalol Hydrochloride 68001-0381
Product NDC
68001-0381- Manufacturer
- Bluepoint Laboratories Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 18, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA207743
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 100 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (68001-381-00)
500 TABLET, FILM COATED in 1 BOTTLE (68001-381-03)