NDC 59746-122 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC59746-122

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Jubilant Cadista Pharmacuticals Inc.
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 (2)

Package NDCDescriptionSince
59746-122-06100 TABLET in 1 BOTTLE (59746-122-06)Jun 4, 2010
59746-122-101000 TABLET in 1 BOTTLE (59746-122-10)Jun 4, 2010

Recalls mentioning this NDC

Other Meclizine Hydrochloride products