Package 85509-1581-1

Brand: diclofenac sodium

Generic: diclofenac sodium topical
NDC Package

Package Facts

Identity

Package NDC 85509-1581-1
Digits Only 8550915811
Product NDC 85509-1581
Description

1 TUBE in 1 CARTON (85509-1581-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-07-21
Brand diclofenac sodium
Generic diclofenac sodium topical
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3a645e5d-e1e4-6f2a-e063-6394a90a4ddc", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["3a63e26f-27d7-9a25-e063-6294a90a55fe"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (85509-1581-1)  / 100 g in 1 TUBE", "package_ndc": "85509-1581-1", "marketing_start_date": "20250721"}], "brand_name": "Diclofenac Sodium", "product_id": "85509-1581_3a645e5d-e1e4-6f2a-e063-6394a90a4ddc", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-1581", "generic_name": "Diclofenac Sodium Topical", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA212351", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}