Package 63029-905-10

Brand: dramamine - n

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63029-905-10
Digits Only 6302990510
Product NDC 63029-905
Description

2 BLISTER PACK in 1 BOX (63029-905-10) / 5 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand dramamine - n
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "101152a8-cb8e-4f6f-b52a-6667b6343a24", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666", "2110527"], "spl_set_id": ["7fec7791-c242-4e43-8184-32820e657afb"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (63029-905-10)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "63029-905-10", "marketing_start_date": "20180115"}], "brand_name": "DRAMAMINE - N", "product_id": "63029-905_101152a8-cb8e-4f6f-b52a-6667b6343a24", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-905", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE - N", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}