NDC 68071-3878 – Labetalol Hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3878
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- NuCare Pharmaceuticals , Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209603
- Marketed since
- May 27, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3878-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3878-9) | Jul 28, 2025 |
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