NDC 0409-0125 – Labetalol Hydrochloride
Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous
Product NDC0409-0125
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA075240
- Marketed since
- August 7, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 0409-0125-25 | 25 VIAL, MULTI-DOSE in 1 TRAY (0409-0125-25) / 20 mL in 1 VIAL, MULTI-DOSE (0409-0125-01) | Aug 7, 2023 |
Recalls mentioning this NDC
- D-0576-2018 Mar 14, 2018 · Class II
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal. - D-1424-2014 Jul 16, 2014 · Class II
Presence of Particulate Matter; metal embedded in the glass vial and visible particles floating in the solution
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