NDC 67046-1693 – Labetalol Hydrochloride
Labetalol Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC67046-1693
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Coupler LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074787
- Marketed since
- August 18, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67046-1693-3 | 30 TABLET in 1 BLISTER PACK (67046-1693-3) | Aug 18, 2026 |
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