NDC 11534-206 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC11534-206
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- Sunrise Pharmaceutical, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207121
- Marketed since
- May 1, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 11534-206-01 | 100 TABLET, FILM COATED in 1 BOTTLE (11534-206-01) | May 1, 2024 |
| 11534-206-03 | 1000 TABLET, FILM COATED in 1 BOTTLE (11534-206-03) | May 1, 2024 |
| 11534-206-04 | 500 TABLET, FILM COATED in 1 BOTTLE (11534-206-04) | Jan 10, 2025 |
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