Meclizine Hydrochloride 00904-7375
Product NDC
00904-7375- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 22, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA201451
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Meclizine Hydrochloride | 12.5 mg/1 |
Drug Class
Antiemetic [EPC]Emesis Suppression [PE]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-7375-61) / 1 TABLET in 1 BLISTER PACK