Package 80425-0056-1

Brand: diclofenac dr

Generic: diclofenac
NDC Package

Package Facts

Identity

Package NDC 80425-0056-1
Digits Only 8042500561
Product NDC 80425-0056
Product ID 80425-0056_2a98d0b7-639a-da12-e063-6294a90a2a7e
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0056-1)

Marketing

Marketing Status
Marketed Since 2008-08-19
Brand diclofenac dr
Generic diclofenac
Sample Package No

Linked Drug Pages (1)

Diclofenac DR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a98d0b7-639a-da12-e063-6294a90a2a7e", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["af8a30fb-ead8-7e29-e053-2a95a90a040f"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0056-1)", "package_ndc": "80425-0056-1", "marketing_start_date": "20080819"}], "brand_name": "Diclofenac DR", "product_id": "80425-0056_2a98d0b7-639a-da12-e063-6294a90a2a7e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0056", "generic_name": "Diclofenac", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac", "brand_name_suffix": "DR", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA077863", "marketing_category": "ANDA", "marketing_start_date": "20080819", "listing_expiration_date": "20261231"}