Package 11673-909-75

Brand: up and up naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 11673-909-75
Digits Only 1167390975
Product NDC 11673-909
Product ID 11673-909_90510c27-046d-456c-a8e1-68d25dd33c09
Description

90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)

Marketing

Marketing Status
Marketed Since 2022-02-10
Brand up and up naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

up and up naproxen sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "90510c27-046d-456c-a8e1-68d25dd33c09", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b0e98603-94e9-474a-88a0-22042f461271"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)", "package_ndc": "11673-909-75", "marketing_start_date": "20220210"}], "brand_name": "up and up naproxen sodium", "product_id": "11673-909_90510c27-046d-456c-a8e1-68d25dd33c09", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-909", "generic_name": "naproxen sodium", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20200214", "listing_expiration_date": "20261231"}