NDC 0409-2339 – Labetalol Hydrochloride
Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous
Product NDC0409-2339
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA075239
- Marketed since
- October 18, 2005
- 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 |
|---|---|---|
| 0409-2339-34 | 10 CARTON in 1 PACKAGE (0409-2339-34) / 1 CARTRIDGE in 1 CARTON / 4 mL in 1 CARTRIDGE (0409-2339-24) | Oct 18, 2005 |
Recalls mentioning this NDC
- D-0565-2024 Jul 3, 2024 · Class II
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
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