NDC 36000-322 – Labetalol Hydrochloride
Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous
Product NDC36000-322
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Baxter Healthcare Corporation
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA076051
- Marketed since
- January 26, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 5 mg/mL
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 36000-322-02 | 1 VIAL in 1 CARTON (36000-322-02) / 20 mL in 1 VIAL (36000-322-01) | Jan 26, 2021 |
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