Package 80267-001-71
Brand: betr headache pain relief
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
80267-001-71
Digits Only
8026700171
Product NDC
80267-001
Description
1 BOTTLE in 1 CARTON (80267-001-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
betr headache pain relief
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eaf6d2fc-ebcb-4d11-8e3f-a494f0f7920b", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["eaf6d2fc-ebcb-4d11-8e3f-a494f0f7920b"], "manufacturer_name": ["Live Betr LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (80267-001-71) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "80267-001-71", "marketing_start_date": "20210209"}], "brand_name": "betr headache pain relief", "product_id": "80267-001_eaf6d2fc-ebcb-4d11-8e3f-a494f0f7920b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80267-001", "generic_name": "naproxen sodium", "labeler_name": "Live Betr LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "betr headache pain relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20210209", "listing_expiration_date": "20261231"}