Labetalol Hydrochloride 67296-2114
Product NDC
67296-2114- Manufacturer
- Redpharm Drug
- 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 | 300 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
21 TABLET, FILM COATED in 1 BOTTLE (67296-2114-2)
60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)