NDC 71205-416 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-416

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040659
Marketed since
June 4, 2010
Listing expires
December 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71205-416-1010 TABLET in 1 BOTTLE (71205-416-10)Mar 3, 2020
71205-416-3030 TABLET in 1 BOTTLE (71205-416-30)Mar 3, 2020
71205-416-6060 TABLET in 1 BOTTLE (71205-416-60)Mar 3, 2020
71205-416-9090 TABLET in 1 BOTTLE (71205-416-90)Mar 3, 2020

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