Package 63029-914-12

Brand: dramamine

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63029-914-12
Digits Only 6302991412
Product NDC 63029-914
Product ID 63029-914_46c83b4e-9f3a-4c67-a759-864e16c5506a
Description

1 BLISTER PACK in 1 BOX (63029-914-12) / 12 TABLET, CHEWABLE in 1 BLISTER PACK

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": "46c83b4e-9f3a-4c67-a759-864e16c5506a", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632", "2176732"], "spl_set_id": ["fdcbcc4e-9370-4975-8905-1f12c73fdc8c"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX (63029-914-12)  / 12 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "63029-914-12", "marketing_start_date": "20260202"}], "brand_name": "DRAMAMINE", "product_id": "63029-914_46c83b4e-9f3a-4c67-a759-864e16c5506a", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-914", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260202", "listing_expiration_date": "20261231"}