NDC 68788-4170 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4170

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202640
Marketed since
August 3, 2026
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
68788-4170-110 TABLET in 1 BOTTLE (68788-4170-1)Aug 3, 2026
68788-4170-330 TABLET in 1 BOTTLE (68788-4170-3)Aug 3, 2026

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