NDC 58657-603 – Labetalol Hydrochloride
Labetalol 200 mg/1 · Tablet, Film Coated · Oral
Product NDC58657-603
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Method Pharmaceuticals, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075215
- Marketed since
- November 22, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol 200 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 58657-603-01 | 100 TABLET, FILM COATED in 1 BOTTLE (58657-603-01) | Nov 22, 2019 |
| 58657-603-50 | 500 TABLET, FILM COATED in 1 BOTTLE (58657-603-50) | Nov 22, 2019 |
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