NDC 71335-0503 – Meclizine Hydrochloride
Meclizine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC71335-0503
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrocloride
- 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 25 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0503-0 | 14 TABLET in 1 BOTTLE (71335-0503-0) | Feb 23, 2022 |
| 71335-0503-1 | 90 TABLET in 1 BOTTLE (71335-0503-1) | Feb 23, 2022 |
| 71335-0503-2 | 30 TABLET in 1 BOTTLE (71335-0503-2) | Feb 23, 2022 |
| 71335-0503-3 | 25 TABLET in 1 BOTTLE (71335-0503-3) | Feb 23, 2022 |
| 71335-0503-4 | 20 TABLET in 1 BOTTLE (71335-0503-4) | Feb 23, 2022 |
| 71335-0503-5 | 40 TABLET in 1 BOTTLE (71335-0503-5) | Feb 23, 2022 |
| 71335-0503-6 | 60 TABLET in 1 BOTTLE (71335-0503-6) | Feb 23, 2022 |
| 71335-0503-7 | 120 TABLET in 1 BOTTLE (71335-0503-7) | Feb 23, 2022 |
| 71335-0503-8 | 10 TABLET in 1 BOTTLE (71335-0503-8) | Feb 23, 2022 |
| 71335-0503-9 | 100 TABLET in 1 BOTTLE (71335-0503-9) | Feb 23, 2022 |
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