NDC 70710-1161 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC70710-1161
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA213957
- Marketed since
- October 29, 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1161-0 | 1000 TABLET in 1 BOTTLE (70710-1161-0) | Oct 29, 2020 |
| 70710-1161-1 | 100 TABLET in 1 BOTTLE (70710-1161-1) | Oct 29, 2020 |
| 70710-1161-3 | 30 TABLET in 1 BOTTLE (70710-1161-3) | Oct 29, 2020 |
| 70710-1161-4 | 10 BLISTER PACK in 1 CARTON (70710-1161-4) / 10 TABLET in 1 BLISTER PACK (70710-1161-2) | Oct 29, 2020 |
| 70710-1161-9 | 90 TABLET in 1 BOTTLE (70710-1161-9) | Oct 29, 2020 |
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