Labetalol Hydrochloride 68382-0800
Product NDC
68382-0800- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA207743
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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(4)
100 TABLET, FILM COATED in 1 BOTTLE (68382-800-01)
500 TABLET, FILM COATED in 1 BOTTLE (68382-800-05)
30 TABLET, FILM COATED in 1 BOTTLE (68382-800-06)
90 TABLET, FILM COATED in 1 BOTTLE (68382-800-16)