Labetalol Hydrochloride 50090-6778
Product NDC
50090-6778- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 3, 1998
- Listing Expires
- December 31, 2026
- Application
- ANDA075133
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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(1)
90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)