Labetalol Hydrochloride 71335-2057
Product NDC
71335-2057- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 22, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA075215
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol | 200 mg/1 |
Drug Class
beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (71335-2057-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-2057-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-2057-3)