Package 67046-1482-3
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
67046-1482-3
Digits Only
6704614823
Product NDC
67046-1482
Description
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1482-3)
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": ["ORAL"], "spl_id": "2ce0666b-491c-9ec6-e063-6394a90a9d02", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["2ce0741a-7bc7-8aec-e063-6294a90ae9ef"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1482-3)", "package_ndc": "67046-1482-3", "marketing_start_date": "20250129"}], "brand_name": "Diclofenac Sodium", "product_id": "67046-1482_2ce0666b-491c-9ec6-e063-6394a90a9d02", "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": "67046-1482", "generic_name": "Diclofenac Sodium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA077863", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}