Labetalol Hydrochloride 29300-0254
Product NDC
29300-0254- Manufacturer
- Unichem Pharmaceuticals (usa), Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA212719
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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)
100 TABLET, FILM COATED in 1 BOTTLE (29300-254-01)
500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)