Package 0904-6772-12

Brand: dimenhydrinate

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 0904-6772-12
Digits Only 0904677212
Product NDC 0904-6772
Product ID 0904-6772_3c44729b-0a55-8eaf-e063-6394a90a5ba4
Description

1 BLISTER PACK in 1 CARTON (0904-6772-12) / 12 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2028-08-31
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": "3c44729b-0a55-8eaf-e063-6394a90a5ba4", "openfda": {"upc": ["0309046772125"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["78d22836-a442-7c0c-e053-2991aa0a62f3"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0904-6772-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6772-12", "marketing_end_date": "20280831", "marketing_start_date": "20190214"}], "brand_name": "Dimenhydrinate", "product_id": "0904-6772_3c44729b-0a55-8eaf-e063-6394a90a5ba4", "dosage_form": "TABLET", "product_ndc": "0904-6772", "generic_name": "Dimenhydrinate", "labeler_name": "Major Pharmaceuticals", "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": "20280831", "marketing_start_date": "20190214"}