NDC 82868-058 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82868-058

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201451
Marketed since
June 11, 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
82868-058-2020 TABLET in 1 BOTTLE, PLASTIC (82868-058-20)Jun 27, 2025
82868-058-3030 TABLET in 1 BOTTLE, PLASTIC (82868-058-30)Jun 11, 2024

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