NDC 70518-4201 – Labetalol Hydrochloride
Labetalol 100 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4201
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075215
- Marketed since
- October 2, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4201-0 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0) | Oct 2, 2024 |
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