NDC 71335-0153 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC71335-0153
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040659
- Marketed since
- June 4, 2010
- Marketing end
- October 31, 2026
- Pharmacologic class
- Antiemetic
Active ingredients
- Meclizine Hydrochloride 12.5 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0153-1 | 30 TABLET in 1 BOTTLE (71335-0153-1) | Feb 23, 2022 |
| 71335-0153-2 | 60 TABLET in 1 BOTTLE (71335-0153-2) | Feb 23, 2022 |
| 71335-0153-3 | 90 TABLET in 1 BOTTLE (71335-0153-3) | Feb 23, 2022 |
| 71335-0153-4 | 28 TABLET in 1 BOTTLE (71335-0153-4) | Feb 23, 2022 |
| 71335-0153-5 | 20 TABLET in 1 BOTTLE (71335-0153-5) | Feb 23, 2022 |
| 71335-0153-6 | 120 TABLET in 1 BOTTLE (71335-0153-6) | Feb 23, 2022 |
| 71335-0153-7 | 100 TABLET in 1 BOTTLE (71335-0153-7) | Feb 23, 2022 |
| 71335-0153-8 | 10 TABLET in 1 BOTTLE (71335-0153-8) | Sep 11, 2025 |
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