NDC 63629-1856 – Hydroxyzine hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-1856
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 25 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 63629-1856-1 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1856-1) | Sep 14, 2015 |
| 63629-1856-2 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-1856-2) | Aug 20, 2015 |
| 63629-1856-3 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-1856-3) | Mar 6, 2015 |
| 63629-1856-4 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-1856-4) | Aug 15, 2024 |
| 63629-1856-5 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-1856-5) | Oct 13, 2023 |
| 63629-1856-6 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-1856-6) | Jan 4, 2017 |
| 63629-1856-7 | 19 TABLET, FILM COATED in 1 BOTTLE (63629-1856-7) | Aug 15, 2024 |
| 63629-1856-8 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-1856-8) | Aug 15, 2024 |
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