Package 0363-0938-82

Brand: all day pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 0363-0938-82
Digits Only 0363093882
Product NDC 0363-0938
Product ID 0363-0938_020d7f84-045c-47f3-88f9-b153a6d43ab2
Description

200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)

Marketing

Marketing Status
Marketed Since 2014-07-31
Brand all day pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

all day pain relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "020d7f84-045c-47f3-88f9-b153a6d43ab2", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8ea540bf-4958-41f9-980f-5936c074a51d"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)", "package_ndc": "0363-0938-82", "marketing_start_date": "20140731"}], "brand_name": "all day pain relief", "product_id": "0363-0938_020d7f84-045c-47f3-88f9-b153a6d43ab2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-0938", "generic_name": "Naproxen Sodium", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "all day pain relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "200 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140731", "listing_expiration_date": "20261231"}