Package 63029-912-04

Brand: dramamine

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63029-912-04
Digits Only 6302991204
Product NDC 63029-912
Product ID 63029-912_871f81c0-8d71-4ff5-8317-9a1f74ba7b83
Description

4 POWDER in 1 BOX (63029-912-04)

Marketing

Marketing Status
Marketed Since 2026-02-02
Brand dramamine
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

DRAMAMINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "871f81c0-8d71-4ff5-8317-9a1f74ba7b83", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["2734132", "2734137"], "spl_set_id": ["6efd3473-ee14-4ee0-8a58-d15a64a9224a"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 POWDER in 1 BOX (63029-912-04)", "package_ndc": "63029-912-04", "marketing_start_date": "20260202"}], "brand_name": "DRAMAMINE", "product_id": "63029-912_871f81c0-8d71-4ff5-8317-9a1f74ba7b83", "dosage_form": "POWDER", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-912", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE", "active_ingredients": [{"name": "MECLIZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260202", "listing_expiration_date": "20261231"}