NDC 0093-5061 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-5061
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 · ANDA088618
- Marketed since
- October 9, 2012
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 0093-5061-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5061-01) | Oct 9, 2012 |
| 0093-5061-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05) | Oct 10, 2012 |
| 0093-5061-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (0093-5061-10) | Oct 11, 2012 |
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