NDC 72888-468 – Labetalol Hydrochloride
Labetalol Hydrochloride 300 mg/1 · Tablet, Film Coated · Oral
Product NDC72888-468
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Advagen Pharma Ltd
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211953
- Marketed since
- May 20, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72888-468-01 | 500 TABLET, FILM COATED in 1 BOTTLE (72888-468-01) | May 20, 2025 |
| 72888-468-02 | 100 TABLET, FILM COATED in 1 BOTTLE (72888-468-02) | May 20, 2025 |
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