Meclizine Hydrochloride 42708-0127
Product NDC
42708-0127- Manufacturer
- Qpharma Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 12, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA201451
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Meclizine Hydrochloride | 25 mg/1 |
Drug Class
Antiemetic [EPC]Emesis Suppression [PE]
Packaging Options(1)
30 TABLET in 1 BOTTLE (42708-127-30)