Package 63187-791-15

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 63187-791-15
Digits Only 6318779115
Product NDC 63187-791
Description

150 mL in 1 BOTTLE (63187-791-15)

Marketing

Marketing Status
Marketed Since 2016-12-01
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TRANSDERMAL"], "spl_id": "7dee7971-4694-409c-b8fa-847074a41234", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["20107264-e533-4de9-9a37-59fde7981c92"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (63187-791-15)", "package_ndc": "63187-791-15", "marketing_start_date": "20161201"}], "brand_name": "Diclofenac Sodium", "product_id": "63187-791_7dee7971-4694-409c-b8fa-847074a41234", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-791", "generic_name": "Diclofenac Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA204132", "marketing_category": "ANDA", "marketing_start_date": "20150820", "listing_expiration_date": "20261231"}