Package 0363-1980-08

Brand: motion sickness relief

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 0363-1980-08
Digits Only 0363198008
Product NDC 0363-1980
Description

4 BLISTER PACK in 1 CARTON (0363-1980-08) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-10-22
Brand motion sickness relief
Generic dimenhydrinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "74bddf47-94e8-4d1f-8015-ec6a52892a4e", "openfda": {"unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["ace7eba4-e033-48f5-8533-c3ea9dfc32b0"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-1980-08)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "0363-1980-08", "marketing_start_date": "20211022"}], "brand_name": "Motion Sickness Relief", "product_id": "0363-1980_74bddf47-94e8-4d1f-8015-ec6a52892a4e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-1980", "generic_name": "Dimenhydrinate", "labeler_name": "Walgreen Company", "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": "20211022", "listing_expiration_date": "20261231"}