NDC 72162-2513 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-2513
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA087871
- Marketed since
- October 7, 2021
- 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 |
|---|---|---|
| 72162-2513-0 | 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2513-0) | May 23, 2025 |
| 72162-2513-1 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2513-1) | May 23, 2025 |
| 72162-2513-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2513-5) | May 23, 2025 |
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