NDC 60687-730 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC60687-730

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201451
Marketed since
April 20, 2023
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
60687-730-01100 BLISTER PACK in 1 CARTON (60687-730-01) / 1 TABLET in 1 BLISTER PACK (60687-730-11)Apr 20, 2023
60687-730-6550 BLISTER PACK in 1 CARTON (60687-730-65) / 1 TABLET in 1 BLISTER PACK (60687-730-11)Feb 7, 2024

Recalls mentioning this NDC

Other Meclizine Hydrochloride products