Labetalol Hydrochloride 62135-0791
Product NDC
62135-0791- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 22, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA074787
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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 in 1 BOTTLE (62135-791-60)