Package 80425-0102-3

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 80425-0102-3
Digits Only 8042501023
Product NDC 80425-0102
Product ID 80425-0102_2a9968c3-c1b8-9ce1-e063-6294a90a8051
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3)

Marketing

Marketing Status
Marketed Since 2010-12-31
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a9968c3-c1b8-9ce1-e063-6294a90a8051", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["b3dbd981-453c-645f-e053-2a95a90aec3c"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-2)", "package_ndc": "80425-0102-2", "marketing_start_date": "20101231"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3)", "package_ndc": "80425-0102-3", "marketing_start_date": "20101231"}], "brand_name": "Diclofenac Sodium", "product_id": "80425-0102_2a9968c3-c1b8-9ce1-e063-6294a90a8051", "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": "80425-0102", "generic_name": "Diclofenac Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA090066", "marketing_category": "ANDA", "marketing_start_date": "20101231", "listing_expiration_date": "20261231"}