NDC 72162-1333 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-1333
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040602
- Marketed since
- March 31, 2015
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1333-2 | 20 TABLET, FILM COATED in 1 BOTTLE (72162-1333-2) | Apr 8, 2024 |
| 72162-1333-3 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1333-3) | Apr 8, 2024 |
| 72162-1333-4 | 15 TABLET, FILM COATED in 1 BOTTLE (72162-1333-4) | Apr 8, 2024 |
| 72162-1333-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-1333-5) | Apr 8, 2024 |
| 72162-1333-6 | 60 TABLET, FILM COATED in 1 BOTTLE (72162-1333-6) | Apr 8, 2024 |
| 72162-1333-8 | 10 TABLET, FILM COATED in 1 BOTTLE (72162-1333-8) | Apr 8, 2024 |
| 72162-1333-9 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-1333-9) | Apr 8, 2024 |
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