NDC 71205-332 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-332
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040604
- Marketed since
- March 31, 2015
- 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 |
|---|---|---|
| 71205-332-15 | 15 TABLET, FILM COATED in 1 BOTTLE (71205-332-15) | Sep 1, 2019 |
| 71205-332-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-332-20) | Sep 1, 2019 |
| 71205-332-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-332-30) | Sep 1, 2019 |
| 71205-332-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-332-60) | Sep 1, 2019 |
| 71205-332-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-332-90) | Sep 1, 2019 |
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