NDC 68071-2380 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2380

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA010721
Marketed since
January 15, 2020
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68071-2380-220 TABLET in 1 BOTTLE (68071-2380-2)Mar 29, 2021
68071-2380-330 TABLET in 1 BOTTLE (68071-2380-3)Mar 29, 2021
68071-2380-990 TABLET in 1 BOTTLE (68071-2380-9)Mar 29, 2021

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