Labetalol Hydrochloride 68071-3878
Product NDC
68071-3878- Manufacturer
- Nucare Pharmaceuticals , Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 27, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA209603
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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 (68071-3878-9)