Package 70000-0749-1

Brand: motion sickness relief

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 70000-0749-1
Digits Only 7000007491
Product NDC 70000-0749
Product ID 70000-0749_ee4af78b-7f75-4562-a98b-081503a079af
Description

2 BLISTER PACK in 1 CARTON (70000-0749-1) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-12-05
Brand motion sickness relief
Generic dimenhydrinate
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": "ee4af78b-7f75-4562-a98b-081503a079af", "openfda": {"upc": ["0096295145588"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["ce83a868-bdd8-4c77-9bc0-664133028f75"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70000-0749-1)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "70000-0749-1", "marketing_start_date": "20251205"}], "brand_name": "Motion Sickness Relief", "product_id": "70000-0749_ee4af78b-7f75-4562-a98b-081503a079af", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70000-0749", "generic_name": "Dimenhydrinate", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness Relief", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251205", "listing_expiration_date": "20261231"}