Labetalol Hydrochloride 33342-0516
Product NDC
33342-0516- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 23, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA217949
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 200 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (33342-516-11)
500 TABLET, FILM COATED in 1 BOTTLE (33342-516-15)