Package 50228-436-10
Brand: naproxen
Generic: naproxenPackage Facts
Identity
Package NDC
50228-436-10
Digits Only
5022843610
Product NDC
50228-436
Description
1000 TABLET in 1 BOTTLE (50228-436-10)
Marketing
Marketing Status
Brand
naproxen
Generic
naproxen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4279d204-4d40-971c-e063-6394a90a2f60", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0350228436106", "0350228435017", "0350228434010", "0350228436014", "0350228434058", "0350228435055", "0350228436052"], "unii": ["57Y76R9ATQ"], "rxcui": ["198012", "198013", "198014"], "spl_set_id": ["81e22c1f-f94d-46e9-8b7d-72dc2518319e"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50228-436-01)", "package_ndc": "50228-436-01", "marketing_start_date": "20200301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50228-436-05)", "package_ndc": "50228-436-05", "marketing_start_date": "20200301"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-436-10)", "package_ndc": "50228-436-10", "marketing_start_date": "20200301"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-436-30)", "package_ndc": "50228-436-30", "marketing_start_date": "20200301"}], "brand_name": "Naproxen", "product_id": "50228-436_4279d204-4d40-971c-e063-6394a90a2f60", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50228-436", "generic_name": "Naproxen", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA212517", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}