NDC 10135-712 – Labetalol Hydrochloride
Labetalol 200 mg/1 · Tablet, Film Coated · Oral
Product NDC10135-712
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol
- Labeler
- Marlex Pharmaceuticals Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075215
- Marketed since
- October 1, 2020
- 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 |
|---|---|---|
| 10135-712-01 | 100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01) | Oct 1, 2020 |
| 10135-712-05 | 500 TABLET, FILM COATED in 1 BOTTLE (10135-712-05) | Oct 1, 2020 |
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