Package 67751-125-01
Brand: flanax pain reliever/fever reducer
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
67751-125-01
Digits Only
6775112501
Product NDC
67751-125
Description
1 PACKET in 1 CARTON (67751-125-01) / 2 TABLET in 1 PACKET
Marketing
Marketing Status
Brand
flanax pain reliever/fever reducer
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f706ab57-bb88-8e63-e053-6394a90a99c0", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f706b406-58f2-9b82-e053-6394a90ab598"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 PACKET in 1 CARTON (67751-125-01) / 2 TABLET in 1 PACKET", "package_ndc": "67751-125-01", "marketing_start_date": "20200720"}], "brand_name": "Flanax Pain Reliever/Fever Reducer", "product_id": "67751-125_f706ab57-bb88-8e63-e053-6394a90a99c0", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67751-125", "generic_name": "Naproxen Sodium", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Flanax Pain Reliever/Fever Reducer", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20200720", "listing_expiration_date": "20261231"}