NDC 16571-115 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC16571-115
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- 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 50 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16571-115-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16571-115-01) | Aug 22, 2023 |
| 16571-115-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (16571-115-10) | Aug 22, 2023 |
| 16571-115-50 | 500 TABLET, FILM COATED in 1 BOTTLE (16571-115-50) | Aug 22, 2023 |
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