NDC 71610-735 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC71610-735
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71610-735-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-735-30) | Sep 14, 2023 |
| 71610-735-53 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-735-53) | Sep 14, 2023 |
| 71610-735-60 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-735-60) | Sep 14, 2023 |
| 71610-735-70 | 120 TABLET, FILM COATED in 1 BOTTLE (71610-735-70) | Sep 14, 2023 |
| 71610-735-80 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-735-80) | Sep 14, 2023 |
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