NDC 68382-800 – Labetalol Hydrochloride
Labetalol Hydrochloride 300 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-800
Product details
- Brand name
- Labetalol Hydrochloride
- Generic name
- Labetalol Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207743
- Marketed since
- December 5, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-800-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-800-01) | Dec 5, 2017 |
| 68382-800-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-800-05) | Dec 5, 2017 |
| 68382-800-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-800-06) | Dec 5, 2017 |
| 68382-800-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-800-16) | Dec 5, 2017 |
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