NDC 10702-010 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC10702-010
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- KVK-Tech, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040786
- Marketed since
- July 24, 2012
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 10702-010-01 | 100 TABLET, FILM COATED in 1 BOTTLE (10702-010-01) | Jul 24, 2012 |
| 10702-010-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (10702-010-10) | Jul 24, 2012 |
| 10702-010-50 | 500 TABLET, FILM COATED in 1 BOTTLE (10702-010-50) | Jul 24, 2012 |
Recalls mentioning this NDC
- D-1032-2014 Jan 29, 2014 · Class II
Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source. - D-1031-2014 Jan 29, 2014 · Class II
Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source. - D-1030-2014 Jan 29, 2014 · Class II
Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.
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