NDC 70518-3768 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-3768

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
June 19, 2023
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
70518-3768-030 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)Jun 19, 2023
70518-3768-190 TABLET in 1 BOTTLE, PLASTIC (70518-3768-1)Sep 16, 2026

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