NDC 71205-095 – Labetalol hydrochloride
Labetalol Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-095
Product details
- Brand name
- Labetalol hydrochloride
- Generic name
- Labetalol hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075133
- Marketed since
- August 3, 1998
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Labetalol Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Labetalol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-095-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30) | Aug 1, 2018 |
| 71205-095-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60) | Aug 1, 2018 |
| 71205-095-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90) | Aug 1, 2018 |
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