Package 50844-199-02

Brand: motion sickness relief

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 50844-199-02
Digits Only 5084419902
Product NDC 50844-199
Description

2 BLISTER PACK in 1 CARTON (50844-199-02) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 1992-12-01
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": "5508a574-f890-4292-a91d-23f7a6652e48", "openfda": {"upc": ["0350844199027"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["95aae32f-6b3f-469d-86a5-c201a53f862a"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50844-199-02)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "50844-199-02", "marketing_start_date": "19921201"}], "brand_name": "Motion Sickness Relief", "product_id": "50844-199_5508a574-f890-4292-a91d-23f7a6652e48", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50844-199", "generic_name": "Dimenhydrinate", "labeler_name": "L.N.K. International, Inc.", "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": "19921201", "listing_expiration_date": "20261231"}