NDC 71335-3157 – Meclizine Hydrochloride
Meclizine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC71335-3157
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202640
- Marketed since
- September 14, 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 (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3157-0 | 14 TABLET in 1 BOTTLE (71335-3157-0) | Jul 27, 2026 |
| 71335-3157-1 | 90 TABLET in 1 BOTTLE (71335-3157-1) | Jul 27, 2026 |
| 71335-3157-2 | 30 TABLET in 1 BOTTLE (71335-3157-2) | Jul 27, 2026 |
| 71335-3157-3 | 25 TABLET in 1 BOTTLE (71335-3157-3) | Jul 27, 2026 |
| 71335-3157-4 | 20 TABLET in 1 BOTTLE (71335-3157-4) | Jul 27, 2026 |
| 71335-3157-5 | 40 TABLET in 1 BOTTLE (71335-3157-5) | Jul 27, 2026 |
| 71335-3157-6 | 60 TABLET in 1 BOTTLE (71335-3157-6) | Jul 27, 2026 |
| 71335-3157-7 | 120 TABLET in 1 BOTTLE (71335-3157-7) | Jul 27, 2026 |
| 71335-3157-8 | 10 TABLET in 1 BOTTLE (71335-3157-8) | Jul 27, 2026 |
| 71335-3157-9 | 100 TABLET in 1 BOTTLE (71335-3157-9) | Jul 27, 2026 |
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