NDC 71335-0503 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0503

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrocloride
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 (10)

Package NDCDescriptionSince
71335-0503-014 TABLET in 1 BOTTLE (71335-0503-0)Feb 23, 2022
71335-0503-190 TABLET in 1 BOTTLE (71335-0503-1)Feb 23, 2022
71335-0503-230 TABLET in 1 BOTTLE (71335-0503-2)Feb 23, 2022
71335-0503-325 TABLET in 1 BOTTLE (71335-0503-3)Feb 23, 2022
71335-0503-420 TABLET in 1 BOTTLE (71335-0503-4)Feb 23, 2022
71335-0503-540 TABLET in 1 BOTTLE (71335-0503-5)Feb 23, 2022
71335-0503-660 TABLET in 1 BOTTLE (71335-0503-6)Feb 23, 2022
71335-0503-7120 TABLET in 1 BOTTLE (71335-0503-7)Feb 23, 2022
71335-0503-810 TABLET in 1 BOTTLE (71335-0503-8)Feb 23, 2022
71335-0503-9100 TABLET in 1 BOTTLE (71335-0503-9)Feb 23, 2022

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