NDC 50268-522 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC50268-522

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201451
Marketed since
August 8, 2013
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50268-522-1550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-522-15) / 1 TABLET in 1 BLISTER PACK (50268-522-11)Aug 8, 2013

Recalls mentioning this NDC

Other Meclizine Hydrochloride products