NDC 70518-3815 – Meclizine Hydrochloride
Meclizine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC70518-3815
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA010721
- Marketed since
- August 2, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiemetic
Active ingredients
- Meclizine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3815-1 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1) | Apr 6, 2024 |
| 70518-3815-2 | 30 TABLET in 1 BLISTER PACK (70518-3815-2) | Feb 7, 2025 |
| 70518-3815-3 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3) | Sep 13, 2025 |
| 70518-3815-4 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4) | Jan 12, 2026 |
| 70518-3815-5 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5) | Feb 17, 2026 |
| 70518-3815-6 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-3815-6) | May 13, 2026 |
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