Package 11673-356-08

Brand: motion sickness relief

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11673-356-08
Digits Only 1167335608
Product NDC 11673-356
Product ID 11673-356_3df6ca6b-8de9-4c46-e063-6294a90ab4e9
Description

1 BLISTER PACK in 1 CARTON (11673-356-08) / 8 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-11-05
Brand motion sickness relief
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Motion Sickness Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3df6ca6b-8de9-4c46-e063-6294a90ab4e9", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["36ba2950-4a09-e5de-e063-6394a90a1771"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11673-356-08)  / 8 TABLET in 1 BLISTER PACK", "package_ndc": "11673-356-08", "marketing_start_date": "20251105"}], "brand_name": "Motion Sickness Relief", "product_id": "11673-356_3df6ca6b-8de9-4c46-e063-6294a90ab4e9", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "11673-356", "generic_name": "Meclizine Hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness Relief", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}