Package 59726-751-20
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
59726-751-20
Digits Only
5972675120
Product NDC
59726-751
Description
1 BOTTLE, PLASTIC in 1 BOX (59726-751-20) / 20 CAPSULE in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
naproxen sodium
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a68267b-0fa0-4b09-b8a8-15f11aaa71f9", "openfda": {"upc": ["0359726751209"], "unii": ["9TN87S3A3C"], "rxcui": ["1112231"], "spl_set_id": ["3bd60171-c073-441a-8d59-c85efee69e07"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-751-20) / 20 CAPSULE in 1 BOTTLE, PLASTIC", "package_ndc": "59726-751-20", "marketing_end_date": "20261231", "marketing_start_date": "20201204"}], "brand_name": "Naproxen Sodium", "product_id": "59726-751_2a68267b-0fa0-4b09-b8a8-15f11aaa71f9", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59726-751", "generic_name": "Naproxen Sodium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA202807", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20201204"}