NDC 70518-4141 – Hydroxyzine Hydrochloride
Hydroxyzine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4141
Product details
- Brand name
- Hydroxyzine Hydrochloride
- Generic name
- Hydroxyzine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217652
- Marketed since
- July 16, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antihistamine
Active ingredients
- Hydroxyzine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4141-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4141-0) | Jul 16, 2024 |
| 70518-4141-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-1) | Mar 26, 2025 |
| 70518-4141-2 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-2) | Jul 15, 2025 |
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