Package 17714-117-01

Brand: meclizine hcl 12.5 mg

Generic: meclizine hcl 12.5 mg
NDC Package

Package Facts

Identity

Package NDC 17714-117-01
Digits Only 1771411701
Product NDC 17714-117
Description

100 TABLET in 1 BOTTLE (17714-117-01)

Marketing

Marketing Status
Marketed Since 2013-07-01
Brand meclizine hcl 12.5 mg
Generic meclizine hcl 12.5 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5cc9755e-6d41-fa9f-e053-2991aa0afbef", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["76efad7e-e765-430f-9232-63553d02f2c5"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-117-01)", "package_ndc": "17714-117-01", "marketing_start_date": "20130701"}], "brand_name": "Meclizine HCL 12.5 mg", "product_id": "17714-117_5cc9755e-6d41-fa9f-e053-2991aa0afbef", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "17714-117", "generic_name": "Meclizine HCL 12.5 mg", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine HCL 12.5 mg", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "part336", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}