Labetalol Hydrochloride 00591-0605
Product NDC
00591-0605- Manufacturer
- Actavis Pharma, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 3, 1998
- Application
- ANDA075133
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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(2)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)