NDC 71335-2451 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2451
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040786
- Marketed since
- July 24, 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2451-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2451-1) | Aug 20, 2024 |
| 71335-2451-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2451-2) | Aug 20, 2024 |
| 71335-2451-3 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2451-3) | Aug 20, 2024 |
| 71335-2451-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2451-4) | Aug 20, 2024 |
| 71335-2451-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2451-5) | Aug 20, 2024 |
| 71335-2451-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2451-6) | Aug 20, 2024 |
| 71335-2451-7 | 19 TABLET, FILM COATED in 1 BOTTLE (71335-2451-7) | Aug 20, 2024 |
| 71335-2451-8 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2451-8) | Aug 20, 2024 |
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