NDC 51655-589 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-589
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA088618
- Marketed since
- February 8, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51655-589-25 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-25) | Jan 10, 2024 |
| 51655-589-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-52) | Jun 27, 2023 |
| 51655-589-53 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-53) | Feb 8, 2021 |
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