Labetalol Hydrochloride 23155-0724
Product NDC
23155-0724- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 22, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA074787
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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(2)
100 TABLET in 1 BOTTLE (23155-724-01)
500 TABLET in 1 BOTTLE (23155-724-05)