Package 49035-981-12

Brand: motion sickness relief

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 49035-981-12
Digits Only 4903598112
Product NDC 49035-981
Description

100 TABLET in 1 BOTTLE, PLASTIC (49035-981-12)

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": "deff1908-fb73-48ba-b735-a06e60059e01", "openfda": {"upc": ["0681131065740"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["c25a7f2b-0f01-4ec0-8849-f08c23608d1d"], "manufacturer_name": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (49035-981-12)", "package_ndc": "49035-981-12", "marketing_start_date": "19921201"}], "brand_name": "Motion Sickness Relief", "product_id": "49035-981_deff1908-fb73-48ba-b735-a06e60059e01", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "49035-981", "generic_name": "Dimenhydrinate", "labeler_name": "Wal-Mart Stores 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": "20271231"}