NDC 68001-701 – Labetalol Hydrochloride
Labetalol Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC68001-701
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074787
- Marketed since
- March 15, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68001-701-00 | 100 TABLET in 1 BOTTLE (68001-701-00) | Mar 15, 2026 |
| 68001-701-03 | 500 TABLET in 1 BOTTLE (68001-701-03) | Mar 15, 2026 |
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