Package 63868-091-50

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63868-091-50
Digits Only 6386809150
Product NDC 63868-091
Description

50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63868-091-50)

Marketing

Marketing Status
Marketed Since 2002-04-30
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": "2a40efa3-1400-3500-e063-6394a90a0b3b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["ded10c13-8a4e-469d-8b34-0d6566be016c"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63868-091-01)", "package_ndc": "63868-091-01", "marketing_start_date": "20020430"}, {"sample": false, "description": "50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63868-091-50)", "package_ndc": "63868-091-50", "marketing_start_date": "20020430"}], "brand_name": "Acetaminophen", "product_id": "63868-091_2a40efa3-1400-3500-e063-6394a90a0b3b", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "63868-091", "generic_name": "Acetaminophen", "labeler_name": "Chain Drug Marketing Association 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": "20020430", "listing_expiration_date": "20261231"}