NDC 68071-3017 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3017

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrocloride
Labeler
NuCare Pharmaceuticals,Inc.
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 (6)

Package NDCDescriptionSince
68071-3017-112 TABLET in 1 BOTTLE (68071-3017-1)Feb 7, 2018
68071-3017-220 TABLET in 1 BOTTLE (68071-3017-2)Feb 7, 2018
68071-3017-330 TABLET in 1 BOTTLE (68071-3017-3)Feb 7, 2018
68071-3017-660 TABLET in 1 BOTTLE (68071-3017-6)Feb 7, 2018
68071-3017-710 TABLET in 1 BOTTLE (68071-3017-7)Feb 7, 2018
68071-3017-990 TABLET in 1 BOTTLE (68071-3017-9)Feb 7, 2018

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