NDC 42806-328 – Labetalol Hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC42806-328
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Epic Pharma, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212990
- Marketed since
- September 30, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 42806-328-01 | 100 TABLET in 1 BOTTLE (42806-328-01) | Sep 30, 2021 |
| 42806-328-05 | 500 TABLET in 1 BOTTLE (42806-328-05) | Sep 30, 2021 |
| 42806-328-10 | 1000 TABLET in 1 BOTTLE (42806-328-10) | Sep 30, 2021 |
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