NDC 24658-781 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC24658-781
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040604
- Marketed since
- July 21, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 24658-781-05 | 500 TABLET, FILM COATED in 1 BOTTLE (24658-781-05) | Oct 24, 2024 |
| 24658-781-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (24658-781-10) | Jul 21, 2021 |
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