NDC 68788-8707 – Hydroxyzine Hydrochloride
Hydroxyzine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8707
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217652
- Marketed since
- July 1, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8707-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8707-3) | Jul 1, 2024 |
| 68788-8707-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8707-6) | Jul 1, 2024 |
| 68788-8707-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8707-9) | Jul 1, 2024 |
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