Package 82501-1576-1

Brand: pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 82501-1576-1
Digits Only 8250115761
Product NDC 82501-1576
Product ID 82501-1576_29ba15a4-8de5-e97f-e063-6394a90a6c9a
Description

100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)

Marketing

Marketing Status
Marketed Since 2022-05-30
Brand pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29ba15a4-8de5-e97f-e063-6394a90a6c9a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["ae4bfa8c-ae41-4fcd-b584-872cc4d37683"], "manufacturer_name": ["Gobrands, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)", "package_ndc": "82501-1576-1", "marketing_start_date": "20220530"}], "brand_name": "Pain Relief", "product_id": "82501-1576_29ba15a4-8de5-e97f-e063-6394a90a6c9a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82501-1576", "generic_name": "Naproxen Sodium", "labeler_name": "Gobrands, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20220530", "listing_expiration_date": "20261231"}