NDC 71335-0153 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0153

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040659
Marketed since
June 4, 2010
Marketing end
October 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0153-130 TABLET in 1 BOTTLE (71335-0153-1)Feb 23, 2022
71335-0153-260 TABLET in 1 BOTTLE (71335-0153-2)Feb 23, 2022
71335-0153-390 TABLET in 1 BOTTLE (71335-0153-3)Feb 23, 2022
71335-0153-428 TABLET in 1 BOTTLE (71335-0153-4)Feb 23, 2022
71335-0153-520 TABLET in 1 BOTTLE (71335-0153-5)Feb 23, 2022
71335-0153-6120 TABLET in 1 BOTTLE (71335-0153-6)Feb 23, 2022
71335-0153-7100 TABLET in 1 BOTTLE (71335-0153-7)Feb 23, 2022
71335-0153-810 TABLET in 1 BOTTLE (71335-0153-8)Sep 11, 2025

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