NDC 71335-1121 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1121
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040600
- Marketed since
- March 31, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1121-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1121-1) | Mar 7, 2019 |
| 71335-1121-2 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1121-2) | Mar 7, 2019 |
| 71335-1121-3 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1121-3) | Mar 7, 2019 |
| 71335-1121-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1121-4) | Apr 2, 2024 |
| 71335-1121-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1121-5) | Mar 7, 2019 |
| 71335-1121-6 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1121-6) | Mar 7, 2019 |
| 71335-1121-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1121-7) | Mar 7, 2019 |
| 71335-1121-8 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1121-8) | Mar 7, 2019 |
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