Package 72789-003-60

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 72789-003-60
Digits Only 7278900360
Product NDC 72789-003
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-003-60)

Marketing

Marketing Status
Marketed Since 2019-08-20
Brand naproxen
Generic naproxen
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4030dd59-8cd7-cfbe-e063-6294a90aad75", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789003603"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915"], "spl_set_id": ["2d01e583-670a-46f4-b5f2-3fad46d0376f"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-003-60)", "package_ndc": "72789-003-60", "marketing_start_date": "20190820"}], "brand_name": "Naproxen", "product_id": "72789-003_4030dd59-8cd7-cfbe-e063-6294a90aad75", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-003", "generic_name": "Naproxen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA091432", "marketing_category": "ANDA", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}