Package 0363-9993-21
Brand: acetaminophen
Generic: acetaminophenPackage Facts
Identity
Package NDC
0363-9993-21
Digits Only
0363999321
Product NDC
0363-9993
Description
225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-9993-21)
Marketing
Marketing Status
Brand
acetaminophen
Generic
acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "465302c4-3a36-5be5-e063-6394a90a317d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["8dba6ae0-1bfb-84de-e053-2a95a90aae46"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-9993-15)", "package_ndc": "0363-9993-15", "marketing_start_date": "20190928"}, {"sample": false, "description": "225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-9993-21)", "package_ndc": "0363-9993-21", "marketing_start_date": "20190928"}], "brand_name": "Acetaminophen", "product_id": "0363-9993_465302c4-3a36-5be5-e063-6394a90a317d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "0363-9993", "generic_name": "Acetaminophen", "labeler_name": "WALGREENS CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20190928", "listing_expiration_date": "20261231"}