NDC 0143-9320 – Labetalol Hydrochloride
Labetalol Hydrochloride 5 mg/mL · Injection · Intravenous
Product NDC0143-9320
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA075303
- Marketed since
- November 29, 1999
- 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 |
|---|---|---|
| 0143-9320-01 | 1 VIAL in 1 BOX, UNIT-DOSE (0143-9320-01) / 20 mL in 1 VIAL | Nov 29, 1999 |
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