NDC 71335-2340 – Hydroxyzine hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet · Oral
Product NDC71335-2340
Product details
- Brand name
- Hydroxyzine hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204279
- Marketed since
- August 20, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2340-1 | 30 TABLET in 1 BOTTLE (71335-2340-1) | Jun 27, 2025 |
| 71335-2340-2 | 60 TABLET in 1 BOTTLE (71335-2340-2) | Jun 27, 2025 |
| 71335-2340-3 | 20 TABLET in 1 BOTTLE (71335-2340-3) | Jun 27, 2025 |
| 71335-2340-4 | 100 TABLET in 1 BOTTLE (71335-2340-4) | Jun 27, 2025 |
| 71335-2340-5 | 15 TABLET in 1 BOTTLE (71335-2340-5) | Jun 27, 2025 |
| 71335-2340-6 | 90 TABLET in 1 BOTTLE (71335-2340-6) | Jun 27, 2025 |
| 71335-2340-7 | 19 TABLET in 1 BOTTLE (71335-2340-7) | Jun 27, 2025 |
| 71335-2340-8 | 10 TABLET in 1 BOTTLE (71335-2340-8) | Jun 27, 2025 |
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