Package 50804-198-02

Brand: motion sickness

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 50804-198-02
Digits Only 5080419802
Product NDC 50804-198
Product ID 50804-198_86fc4e4e-9d57-4148-9877-be31360a5a47
Description

2 BLISTER PACK in 1 CARTON (50804-198-02) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-04-07
Brand motion sickness
Generic dimenhydrinate
Sample Package No

Linked Drug Pages (1)

Motion Sickness ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "86fc4e4e-9d57-4148-9877-be31360a5a47", "openfda": {"upc": ["0846036000894"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["fdb683c5-ff7f-4b93-9892-670cf1f29f2a"], "manufacturer_name": ["Geiss, Destin & Dunn Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50804-198-02)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "50804-198-02", "marketing_start_date": "20200407"}], "brand_name": "Motion Sickness", "product_id": "50804-198_86fc4e4e-9d57-4148-9877-be31360a5a47", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50804-198", "generic_name": "Dimenhydrinate", "labeler_name": "Geiss, Destin & Dunn Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200407", "listing_expiration_date": "20261231"}