NDC 71335-3157 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3157

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202640
Marketed since
September 14, 2023
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-3157-014 TABLET in 1 BOTTLE (71335-3157-0)Jul 27, 2026
71335-3157-190 TABLET in 1 BOTTLE (71335-3157-1)Jul 27, 2026
71335-3157-230 TABLET in 1 BOTTLE (71335-3157-2)Jul 27, 2026
71335-3157-325 TABLET in 1 BOTTLE (71335-3157-3)Jul 27, 2026
71335-3157-420 TABLET in 1 BOTTLE (71335-3157-4)Jul 27, 2026
71335-3157-540 TABLET in 1 BOTTLE (71335-3157-5)Jul 27, 2026
71335-3157-660 TABLET in 1 BOTTLE (71335-3157-6)Jul 27, 2026
71335-3157-7120 TABLET in 1 BOTTLE (71335-3157-7)Jul 27, 2026
71335-3157-810 TABLET in 1 BOTTLE (71335-3157-8)Jul 27, 2026
71335-3157-9100 TABLET in 1 BOTTLE (71335-3157-9)Jul 27, 2026

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