Package 0363-0669-01

Brand: extra strength pain reliever

Generic: acetaminophen tablets 500 mg
NDC Package

Package Facts

Identity

Package NDC 0363-0669-01
Digits Only 0363066901
Product NDC 0363-0669
Description

1 BOTTLE in 1 CARTON (0363-0669-01) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-10-13
Brand extra strength pain reliever
Generic acetaminophen tablets 500 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ce99cb7-fea1-5da2-e063-6294a90afc4e", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c25bfe92-0196-0489-e053-2995a90abea1"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0669-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "0363-0669-01", "marketing_start_date": "20211013"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "0363-0669_2ce99cb7-fea1-5da2-e063-6294a90afc4e", "dosage_form": "TABLET", "product_ndc": "0363-0669", "generic_name": "Acetaminophen tablets 500 mg", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211013", "listing_expiration_date": "20261231"}