NDC 70518-3993 – Labetalol Hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3993
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209603
- Marketed since
- January 24, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3993-0 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0) | Jan 24, 2024 |
| 70518-3993-1 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1) | Jan 24, 2024 |
| 70518-3993-2 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2) | Jan 20, 2025 |
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