Meclizine Hydrochloride 82868-0058
Product NDC
82868-0058- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 11, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA201451
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Meclizine Hydrochloride | 25 mg/1 |
Drug Class
Antiemetic [EPC]Emesis Suppression [PE]
Packaging Options(2)
20 TABLET in 1 BOTTLE, PLASTIC (82868-058-20)
30 TABLET in 1 BOTTLE, PLASTIC (82868-058-30)