NDC 71335-0246 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0246
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0246-1 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0246-1) | Oct 4, 2017 |
| 71335-0246-2 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0246-2) | Oct 4, 2017 |
| 71335-0246-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0246-3) | Oct 4, 2017 |
| 71335-0246-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0246-4) | Oct 4, 2017 |
| 71335-0246-5 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0246-5) | Oct 4, 2017 |
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