NDC 50090-6741 – Labetalol Hydrochloride
Labetalol Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-6741
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211953
- Marketed since
- August 18, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-6741-0 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-6741-0) | Oct 13, 2023 |
| 50090-6741-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6741-1) | Oct 13, 2023 |
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