Package 70000-0404-1

Brand: dimenhydrinate

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 70000-0404-1
Digits Only 7000004041
Product NDC 70000-0404
Product ID 70000-0404_4b4343e5-4d4d-6a4a-e063-6394a90ad2bc
Description

1 BLISTER PACK in 1 CARTON (70000-0404-1) / 12 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2029-02-28
Brand dimenhydrinate
Generic dimenhydrinate
Sample Package No

Linked Drug Pages (1)

Dimenhydrinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b4343e5-4d4d-6a4a-e063-6394a90ad2bc", "openfda": {"upc": ["0096295135183"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["7c4adbdb-9bce-0c9c-e053-2a91aa0a8107"], "manufacturer_name": ["LEADER/ Cardinal Health 110, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70000-0404-1)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "70000-0404-1", "marketing_end_date": "20290228", "marketing_start_date": "20190104"}], "brand_name": "Dimenhydrinate", "product_id": "70000-0404_4b4343e5-4d4d-6a4a-e063-6394a90ad2bc", "dosage_form": "TABLET", "product_ndc": "70000-0404", "generic_name": "Dimenhydrinate", "labeler_name": "LEADER/ Cardinal Health 110, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dimenhydrinate", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20290228", "marketing_start_date": "20190104"}