NDC 71335-1872 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC71335-1872
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA010721
- Marketed since
- January 15, 2020
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1872-1 | 30 TABLET in 1 BOTTLE (71335-1872-1) | Jun 28, 2021 |
| 71335-1872-2 | 60 TABLET in 1 BOTTLE (71335-1872-2) | Jun 28, 2021 |
| 71335-1872-3 | 90 TABLET in 1 BOTTLE (71335-1872-3) | Jun 28, 2021 |
| 71335-1872-4 | 28 TABLET in 1 BOTTLE (71335-1872-4) | Jun 28, 2021 |
| 71335-1872-5 | 20 TABLET in 1 BOTTLE (71335-1872-5) | Jun 28, 2021 |
| 71335-1872-6 | 120 TABLET in 1 BOTTLE (71335-1872-6) | Jun 28, 2021 |
| 71335-1872-7 | 100 TABLET in 1 BOTTLE (71335-1872-7) | Jun 28, 2021 |
| 71335-1872-8 | 10 TABLET in 1 BOTTLE (71335-1872-8) | Jun 28, 2021 |
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