Package 85509-1406-1
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
85509-1406-1
Digits Only
8550914061
Product NDC
85509-1406
Description
1 BOTTLE in 1 CARTON (85509-1406-1) / 112 g in 1 BOTTLE
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "41da3d90-4847-0d8f-e063-6294a90aede1", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["1487074"], "spl_set_id": ["41da2e11-58c7-9622-e063-6394a90a9fdb"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (85509-1406-1) / 112 g in 1 BOTTLE", "package_ndc": "85509-1406-1", "marketing_start_date": "20251023"}], "brand_name": "Diclofenac Sodium", "product_id": "85509-1406_41da3d90-4847-0d8f-e063-6294a90aede1", "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": "85509-1406", "generic_name": "Diclofenac Sodium", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "20 mg/g"}], "application_number": "ANDA207714", "marketing_category": "ANDA", "marketing_start_date": "20220509", "listing_expiration_date": "20261231"}