Meclizine Hydrochloride 16571-0663
Product NDC
16571-0663- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 15, 2020
- Listing Expires
- December 31, 2026
- Application
- NDA010721
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Meclizine Hydrochloride | 25 mg/1 |
Drug Class
Antiemetic [EPC]Emesis Suppression [PE]
Packaging Options(1)
100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)