NDC 63629-4929 – Hydroxyzine hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-4929
Product details
- Brand name
- Hydroxyzine hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204279
- Marketed since
- August 20, 2014
- 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 |
|---|---|---|
| 63629-4929-1 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4929-1) | Aug 20, 2014 |
| 63629-4929-2 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-4929-2) | Aug 20, 2014 |
| 63629-4929-3 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4929-3) | Aug 20, 2014 |
| 63629-4929-4 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4929-4) | Aug 20, 2014 |
| 63629-4929-5 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4929-5) | Aug 20, 2014 |
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