Labetalol Hydrochloride 70771-1165
Product NDC
70771-1165- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207743
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 300 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (70771-1165-1)
30 TABLET, FILM COATED in 1 BOTTLE (70771-1165-3)
500 TABLET, FILM COATED in 1 BOTTLE (70771-1165-5)
90 TABLET, FILM COATED in 1 BOTTLE (70771-1165-9)