NDC 16571-660 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16571-660

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA010721
Marketed since
January 15, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

Uses, dosage, side effects and warnings for Meclizine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
16571-660-01100 TABLET in 1 BOTTLE (16571-660-01)Jan 15, 2020
16571-660-50500 TABLET in 1 BOTTLE (16571-660-50)Jan 15, 2020

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