NDC 70377-062 – Labetalol Hydrochloride
Labetalol Hydrochloride 300 mg/1 · Tablet, Film Coated · Oral
Product NDC70377-062
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
- May 27, 2021
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70377-062-11 | 30 TABLET, FILM COATED in 1 BOTTLE (70377-062-11) | May 27, 2021 |
| 70377-062-12 | 100 TABLET, FILM COATED in 1 BOTTLE (70377-062-12) | May 27, 2021 |
| 70377-062-13 | 500 TABLET, FILM COATED in 1 BOTTLE (70377-062-13) | May 27, 2021 |
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