Package 0363-0340-08

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0363-0340-08
Digits Only 0363034008
Product NDC 0363-0340
Description

80 TABLET, EXTENDED RELEASE in 1 BOTTLE (0363-0340-08)

Marketing

Marketing Status
Marketed Since 2016-05-01
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": "1bc5ce72-38f4-43f7-99cc-2b8b4725e15b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["a1cec332-5802-4684-8b7f-6cb98da40e8b"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, EXTENDED RELEASE in 1 BOTTLE (0363-0340-08)", "package_ndc": "0363-0340-08", "marketing_start_date": "20160501"}], "brand_name": "Acetaminophen", "product_id": "0363-0340_1bc5ce72-38f4-43f7-99cc-2b8b4725e15b", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "0363-0340", "generic_name": "Acetaminophen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA078569", "marketing_category": "ANDA", "marketing_start_date": "20160501", "listing_expiration_date": "20261231"}