NDC 0093-5062 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-5062
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA088619
- Marketed since
- October 22, 2012
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-5062-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5062-01) | Mar 11, 2013 |
| 0093-5062-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-5062-05) | Oct 22, 2012 |
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