Package 85509-1911-1
Brand: diclofenac sodium
Generic: diclofenacPackage Facts
Identity
Package NDC
85509-1911-1
Digits Only
8550919111
Product NDC
85509-1911
Description
1 BOTTLE in 1 CARTON (85509-1911-1) / 150 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "41daa6f6-41c5-b81e-e063-6394a90a7516", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["41dab520-5651-a4c5-e063-6394a90a2962"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (85509-1911-1) / 150 mL in 1 BOTTLE", "package_ndc": "85509-1911-1", "marketing_start_date": "20251023"}], "brand_name": "Diclofenac Sodium", "product_id": "85509-1911_41daa6f6-41c5-b81e-e063-6394a90a7516", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-1911", "generic_name": "Diclofenac", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA206116", "marketing_category": "ANDA", "marketing_start_date": "20160902", "listing_expiration_date": "20261231"}