NDC 70518-3499 – Labetalol Hydrochloride
Labetalol Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3499
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211953
- Marketed since
- August 25, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3499-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3499-0) | Aug 25, 2022 |
| 70518-3499-1 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-1) | Sep 20, 2022 |
| 70518-3499-2 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-2) | Sep 20, 2022 |
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