NDC 50090-6778 – Labetalol hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-6778
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 · ANDA075133
- Marketed since
- August 3, 1998
- 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 |
|---|---|---|
| 50090-6778-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0) | Oct 25, 2023 |
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