Package 63029-906-12

Brand: dramamine

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63029-906-12
Digits Only 6302990612
Product NDC 63029-906
Product ID 63029-906_4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4
Description

12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12)

Marketing

Marketing Status
Marketed Since 2019-02-15
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": "4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632", "2176732"], "spl_set_id": ["f8cf751a-9f19-4744-a350-cd22303435ee"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12)", "package_ndc": "63029-906-12", "marketing_start_date": "20190215"}], "brand_name": "DRAMAMINE", "product_id": "63029-906_4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-906", "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": "20190215", "listing_expiration_date": "20261231"}