Package 69842-037-44

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69842-037-44
Digits Only 6984203744
Product NDC 69842-037
Description

400 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-44)

Marketing

Marketing Status
Marketed Since 2020-12-23
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": "3ac76330-16d2-44f6-b013-8683059b83a9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b70beee4-407e-547c-e053-2a95a90af22a"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-35)", "package_ndc": "69842-037-35", "marketing_start_date": "20201223"}, {"sample": false, "description": "400 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-44)", "package_ndc": "69842-037-44", "marketing_start_date": "20201223"}], "brand_name": "Acetaminophen", "product_id": "69842-037_3ac76330-16d2-44f6-b013-8683059b83a9", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "69842-037", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207229", "marketing_category": "ANDA", "marketing_start_date": "20201223", "listing_expiration_date": "20261231"}