Labetalol Hydrochloride 50090-6741
Product NDC
50090-6741- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 18, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA211953
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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)
60 TABLET, FILM COATED in 1 BOTTLE (50090-6741-0)
90 TABLET, FILM COATED in 1 BOTTLE (50090-6741-1)