NDC 71335-1563 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC71335-1563
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
- Listing expires
- December 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1563-1 | 30 TABLET in 1 BOTTLE (71335-1563-1) | Jun 4, 2010 |
| 71335-1563-2 | 60 TABLET in 1 BOTTLE (71335-1563-2) | Jun 4, 2010 |
| 71335-1563-3 | 90 TABLET in 1 BOTTLE (71335-1563-3) | Jun 4, 2010 |
| 71335-1563-4 | 28 TABLET in 1 BOTTLE (71335-1563-4) | Jun 4, 2010 |
| 71335-1563-5 | 20 TABLET in 1 BOTTLE (71335-1563-5) | Jun 4, 2010 |
| 71335-1563-6 | 120 TABLET in 1 BOTTLE (71335-1563-6) | Jun 4, 2010 |
| 71335-1563-7 | 100 TABLET in 1 BOTTLE (71335-1563-7) | Jun 4, 2010 |
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