NDC 71335-3141 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3141

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 (8)

Package NDCDescriptionSince
71335-3141-130 TABLET in 1 BOTTLE (71335-3141-1)Jun 8, 2026
71335-3141-260 TABLET in 1 BOTTLE (71335-3141-2)Jun 8, 2026
71335-3141-390 TABLET in 1 BOTTLE (71335-3141-3)Jun 8, 2026
71335-3141-428 TABLET in 1 BOTTLE (71335-3141-4)Jun 8, 2026
71335-3141-520 TABLET in 1 BOTTLE (71335-3141-5)Jun 8, 2026
71335-3141-6120 TABLET in 1 BOTTLE (71335-3141-6)Jun 8, 2026
71335-3141-7100 TABLET in 1 BOTTLE (71335-3141-7)Jun 8, 2026
71335-3141-810 TABLET in 1 BOTTLE (71335-3141-8)Jun 8, 2026

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