NDC 50090-7332 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-7332
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217652
- Marketed since
- August 22, 2023
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7332-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7332-0) | Oct 15, 2024 |
| 50090-7332-1 | 28 TABLET, FILM COATED in 1 BOTTLE (50090-7332-1) | Oct 19, 2024 |
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