NDC 62135-792 – Labetalol Hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC62135-792
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074787
- Marketed since
- February 22, 2020
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 62135-792-60 | 60 TABLET in 1 BOTTLE (62135-792-60) | Oct 24, 2023 |
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