Labetalol Hydrochloride 71209-0084
Product NDC
71209-0084- Manufacturer
- Cadila Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 5, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA211325
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Labetalol Hydrochloride | 200 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(4)
60 TABLET, FILM COATED in 1 BOTTLE (71209-084-03)
100 TABLET, FILM COATED in 1 BOTTLE (71209-084-05)
500 TABLET, FILM COATED in 1 BOTTLE (71209-084-10)
1000 TABLET, FILM COATED in 1 BOTTLE (71209-084-11)