Package 69790-154-33

Brand: uline acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69790-154-33
Digits Only 6979015433
Product NDC 69790-154
Product ID 69790-154_3e5d8ade-be5f-4cfa-e063-6394a90a99f6
Description

50 PACKET in 1 BOX (69790-154-33) / 2 TABLET, FILM COATED in 1 PACKET

Marketing

Marketing Status
Marketed Since 2024-01-30
Brand uline acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Uline Acetaminophen Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e5d8ade-be5f-4cfa-e063-6394a90a99f6", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["90167594-0a49-2492-e053-2a95a90a1401"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (69790-154-33)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "69790-154-33", "marketing_start_date": "20240130"}], "brand_name": "Uline Acetaminophen Extra Strength", "product_id": "69790-154_3e5d8ade-be5f-4cfa-e063-6394a90a99f6", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69790-154", "generic_name": "acetaminophen", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uline Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240130", "listing_expiration_date": "20261231"}