Meclizine Hydrochloride 16571-0662-01

Package NDC

16571-0662-01

Manufacturer: Rising Pharma Holdings, Inc.
Dosage Form: Tablet
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	50 mg/1

Drug Class

Antiemetic [EPC]Emesis Suppression [PE]

Selected Package

16571-0662-01Selected

100 TABLET in 1 BOTTLE (16571-662-01)