NDC 70518-3815 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-3815

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA010721
Marketed since
August 2, 2023
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
70518-3815-130 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1)Apr 6, 2024
70518-3815-230 TABLET in 1 BLISTER PACK (70518-3815-2)Feb 7, 2025
70518-3815-390 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)Sep 13, 2025
70518-3815-430 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)Jan 12, 2026
70518-3815-510 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)Feb 17, 2026
70518-3815-620 TABLET in 1 BOTTLE, PLASTIC (70518-3815-6)May 13, 2026

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