NDC 68788-8633 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8633

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA010721
Marketed since
April 16, 2024
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
68788-8633-110 TABLET in 1 BOTTLE (68788-8633-1)Apr 16, 2024
68788-8633-330 TABLET in 1 BOTTLE (68788-8633-3)Apr 16, 2024

Other Meclizine Hydrochloride products