NDC 70518-1308 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-1308

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrocloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040659
Marketed since
August 17, 2018
Marketing end
October 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-1308-090 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)Aug 17, 2018

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