NDC 0591-0605 – Labetalol hydrochloride
Labetalol Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC0591-0605
Product details
- Brand name
- Labetalol hydrochloride
- Generic name
- Labetalol hydrochloride
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075133
- Marketed since
- August 3, 1998
- Marketing end
- September 30, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0591-0605-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01) | Aug 3, 1998 |
| 0591-0605-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05) | Aug 3, 1998 |
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