Labetalol Hydrochloride 70377-0062
Product NDC
70377-0062- Manufacturer
- Biocon Pharma Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 27, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA209603
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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(3)
30 TABLET, FILM COATED in 1 BOTTLE (70377-062-11)
100 TABLET, FILM COATED in 1 BOTTLE (70377-062-12)
500 TABLET, FILM COATED in 1 BOTTLE (70377-062-13)