Package 47682-037-50
Brand: belmora flanax
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
47682-037-50
Digits Only
4768203750
Product NDC
47682-037
Description
50 PACKET in 1 BOX (47682-037-50) / 1 TABLET, FILM COATED in 1 PACKET
Marketing
Marketing Status
Brand
belmora flanax
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ebf3deb7-0831-d81b-e053-2a95a90ae3be", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8591ca57-04ee-5053-e053-2991aa0aa4dd"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (47682-037-50) / 1 TABLET, FILM COATED in 1 PACKET", "package_ndc": "47682-037-50", "marketing_start_date": "20081230"}], "brand_name": "Belmora Flanax", "product_id": "47682-037_ebf3deb7-0831-d81b-e053-2a95a90ae3be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "47682-037", "generic_name": "Naproxen Sodium", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Belmora Flanax", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}