Package 65862-515-01

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 65862-515-01
Digits Only 6586251501
Product NDC 65862-515
Product ID 65862-515_a4659cf5-a74b-42b3-968b-a8e4f14f94aa
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-515-01)

Marketing

Marketing Status
Marketed Since 2011-10-31
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a4659cf5-a74b-42b3-968b-a8e4f14f94aa", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849398", "849431"], "spl_set_id": ["37b264f9-b46d-4635-8fab-246b1e08b653"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-515-01)", "package_ndc": "65862-515-01", "marketing_start_date": "20111031"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-515-05)", "package_ndc": "65862-515-05", "marketing_start_date": "20111031"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-515-99)", "package_ndc": "65862-515-99", "marketing_start_date": "20111031"}], "brand_name": "Naproxen Sodium", "product_id": "65862-515_a4659cf5-a74b-42b3-968b-a8e4f14f94aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "65862-515", "generic_name": "Naproxen Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "275 mg/1"}], "application_number": "ANDA200629", "marketing_category": "ANDA", "marketing_start_date": "20111031", "listing_expiration_date": "20261231"}