Package 51655-107-20

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-107-20
Digits Only 5165510720
Product NDC 51655-107
Description

20 TABLET in 1 BOTTLE, PLASTIC (51655-107-20)

Marketing

Marketing Status
Discontinued 2026-10-31
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c3b27e-acb4-6023-e063-6294a90ae95a", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["c443873a-2e89-43b2-b145-dde3dadf7bc0"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-107-20)", "package_ndc": "51655-107-20", "marketing_end_date": "20261031", "marketing_start_date": "20231214"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, DISPENSING (51655-107-52)", "package_ndc": "51655-107-52", "marketing_end_date": "20261031", "marketing_start_date": "20140724"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "51655-107_48c3b27e-acb4-6023-e063-6294a90ae95a", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "51655-107", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20140724"}