NDC 70377-063 – Labetalol Hydrochloride
Labetalol Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC70377-063
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Biocon Pharma Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209603
- Marketed since
- December 2, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 400 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70377-063-11 | 30 TABLET, FILM COATED in 1 BOTTLE (70377-063-11) | Aug 7, 2025 |
| 70377-063-12 | 100 TABLET, FILM COATED in 1 BOTTLE (70377-063-12) | Dec 2, 2024 |
| 70377-063-13 | 500 TABLET, FILM COATED in 1 BOTTLE (70377-063-13) | Dec 2, 2024 |
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