Package 55315-333-50

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 55315-333-50
Digits Only 5531533350
Product NDC 55315-333
Product ID 55315-333_bb89acc6-20df-465f-aca0-424c0d4dc32f
Description

50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55315-333-50)

Marketing

Marketing Status
Marketed Since 2019-12-24
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bb89acc6-20df-465f-aca0-424c0d4dc32f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["070569ec-82b1-4b26-b38b-3fb3caf71f19"], "manufacturer_name": ["Fred's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55315-333-50)", "package_ndc": "55315-333-50", "marketing_start_date": "20191224"}], "brand_name": "Acetaminophen", "product_id": "55315-333_bb89acc6-20df-465f-aca0-424c0d4dc32f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "55315-333", "generic_name": "Acetaminophen", "labeler_name": "Fred's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA076200", "marketing_category": "ANDA", "marketing_start_date": "20040430", "listing_expiration_date": "20261231"}