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NDC 65162-0444-50 Meclizine Hydrochloride 50 mg/1 Details

Meclizine Hydrochloride 50 mg/1

Meclizine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is MECLIZINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Meclizine is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is most effective if taken before symptoms appear.

Related Packages: 65162-0444-50
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Meclizine

Product Information

NDC	65162-0444
Product ID	65162-444_f36cd043-3266-48c7-8eb5-c4eaf937f1aa
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Meclizine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Meclizine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	50
Active Ingredient Units	mg/1
Substance Name	MECLIZINE HYDROCHLORIDE
Labeler Name	Amneal Pharmaceuticals LLC
Pharmaceutical Class	Antiemetic [EPC], Emesis Suppression [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA201451
Listing Certified Through	2024-12-31

Package

NDC 65162-0444-50 (65162044450)

Pricing Information	N/A
NDC Package Code	65162-444-50
Billing NDC	65162044450
Package	500 TABLET in 1 BOTTLE (65162-444-50)
Marketing Start Date	2010-02-12
NDC Exclude Flag	N