NDC 71205-647 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-647

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA010721
Marketed since
January 15, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71205-647-1010 TABLET in 1 BOTTLE (71205-647-10)Mar 23, 2022
71205-647-9090 TABLET in 1 BOTTLE (71205-647-90)Mar 23, 2022

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