NDC 70518-4170 – Hydroxyzine Hydrochloride
Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4170
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
- August 28, 2024
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4170-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0) | Aug 28, 2024 |
| 70518-4170-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1) | Apr 4, 2025 |
| 70518-4170-2 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2) | Jul 8, 2025 |
| 70518-4170-3 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3) | Oct 24, 2025 |
| 70518-4170-4 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-4) | Dec 22, 2025 |
| 70518-4170-5 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-5) | Apr 9, 2026 |
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