NDC 59651-501 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-501
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA087871
- Marketed since
- October 7, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Dihydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 59651-501-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-501-01) | Oct 7, 2021 |
| 59651-501-05 | 500 TABLET, FILM COATED in 1 BOTTLE (59651-501-05) | Oct 7, 2021 |
| 59651-501-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (59651-501-99) | Oct 7, 2021 |
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