Labetalol Hydrochloride 51655-0322
Product NDC
51655-0322- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 25, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA209603
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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(1)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)